(Q38125413)

29 August 2017

title

GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype (English)

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29 August 2017

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1 reference

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Kay W Chang

2

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author name string

Dylan K Chan

series ordinal

1

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29 August 2017

language of work or name

English

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publication date

8 October 2013

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29 August 2017

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29 August 2017

volume

124

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29 August 2017

issue

2

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29 August 2017

page(s)

E34-53

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Newborn hearing screening--a silent revolution

29 August 2017

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Connexin-dependent inter-cellular communication increases invasion and dissemination of Shigella in epithelial cells

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The digenic hypothesis unraveled: the GJB6 del(GJB6-D13S1830) mutation causes allele-specific loss of GJB2 expression in cis.

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Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings.

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Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method

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High carrier frequency of the 35delG deafness mutation in European populations

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Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

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Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT.

21 January 2018

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Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.

21 January 2018

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Connexin-26 gene analysis in hearing-impaired newborns.

21 January 2018

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Connexin26 mutations associated with nonsyndromic hearing loss.

21 January 2018

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

21 January 2018

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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

High frequency hearing loss correlated with mutations in the GJB2 gene.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana

21 January 2018

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Connexin 26 studies in patients with sensorineural hearing loss.

21 January 2018

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Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.

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Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.

21 January 2018

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Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population.

21 January 2018

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Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

21 January 2018

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High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria.

21 January 2018

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Exploring the clinical and epidemiological complexity of GJB2-linked deafness.

21 January 2018

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Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.

21 January 2018

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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 preverbal hearing impairment: mutation prevalence and heterozygosity in a selected population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 gene mutations causing familial hereditary deafness in Turkey.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in the Swiss hearing impaired.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Elevated frequencies of the 35delG allele of the connexin 26 gene in Corsica, France

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2: the spectrum of deafness-causing allele variants and their phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

A genotype-phenotype correlation for GJB2 (connexin 26) deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Large deletion of theGJB6gene in deaf patients heterozygous for theGJB2gene mutation: Genotypic and phenotypic analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Low frequency of deafness-associated GJB2 variants in Kenya and Sudan and novel GJB2 variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Sensorineural hearing loss in Jewish children born in Jerusalem

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 gene mutations in cochlear implant recipients: prevalence and impact on outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Molecular epidemiology of DFNB1 deafness in France

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Connexin 26 (GJB2) gene-related deafness and speech intelligibility after cochlear implantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals

21 January 2018

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Etiologic diagnosis of sensorineural hearing loss in adults.

21 January 2018

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Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counseling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations.

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Audiological features of GJB2 (connexin 26) deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

[Prospects for genetic hearing loss screening: 35delG mutation tracking in a newborn population].

21 January 2018

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https://api.crossref.org/works/10.1002%2FLARY.24332

First molecular screening of deafness in the Altai Republic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of the 35delG mutation in the GJB2 gene of patients with nonsyndromic hearing loss from Croatia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation analysis of the GJB2 (connexin 26) gene in Egypt

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Temporal bone imaging in GJB2 deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations and additional disabilities in a pediatric cochlear implant population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population. Impact on the newborn hearing screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Etiology of severe sensorineural hearing loss in children: independent impact of congenital cytomegalovirus infection and GJB2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Allelic frequencies of the 35delG mutation of the GJB2 gene in different Brazilian regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Correlation between audiometric data and the 35delG mutation in ten patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High incidence of GJB2 mutations during screening of newborns for hearing loss in Austria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Phenotype/genotype correlations in a DFNB1 cohort with ethnical diversity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Spectrum of GJB2 mutations causing deafness in the British Bangladeshi population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in Baluchi population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Infant hearing loss and connexin testing in a diverse population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation in gap and tight junctions in patients with non-syndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation analysis of familial GJB2-related deafness in Iranian Azeri Turkish patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High prevalence of the connexin 26 (GJB2) mutation in Chinese cochlear implant recipients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and GJB6 gene mutations found in Indian probands with congenital hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Correlation between GJB2 mutations and audiological deficits: personal experience.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in patients with nonsyndromic hearing loss from Croatia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

DFNB1-associated deafness in Portuguese cochlear implant users: prevalence and impact on oral outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and GJB6 genes: molecular study and identification of novel GJB2 mutations in the hearing-impaired Argentinean population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Newborn hearing screening and genetic testing in 8974 Brazilian neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Causes of hearing impairment in the Norwegian paediatric cochlear implant program.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

A large cohort study of GJB2 mutations in Japanese hearing loss patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutations of the Connexin 26 gene in families with non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and mitochondrial DNA 1555A>G mutations in students with hearing loss in the Hubei Province of China

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Temporal bone abnormalities in children with GJB2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Determination of the carrier frequencies of selected GJB2 mutations in the Korean population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Comprehensive diagnostic battery for evaluating sensorineural hearing loss in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Clinical comparison of hearing-impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 allele variants and the associated audiologic features identified in Chinese patients with less severe idiopathic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Novel connexin 30 and connexin 26 mutational spectrum in patients with progressive sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Spectrum of genetic changes in patients with non-syndromic hearing impairment and extremely high carrier frequency of 35delG GJB2 mutation in Belarus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Etiology of unilateral hearing loss in a national hereditary deafness repository

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in east Greenland

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Etiologic diagnosis of nonsyndromic genetic hearing loss in adult vs pediatric populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Genetic Screening of GJB2 and SLC26A4 in Korean Cochlear Implantees: Experience of Soree Ear Clinic

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Mutation detection in GJB2 gene among Malays with non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

V37I connexin 26 allele in patients with sensorineural hearing loss: Evidence of its pathogenicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

Epidemiological study of nonsyndromic hearing loss in Sicilian newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FLARY.24332

21 January 2018

Identifiers

DOI

10.1002/LARY.24332

1 reference

29 August 2017

1 reference