(Q30898157)

27 June 2017

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title

Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency (English)

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27 June 2017

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Nejat Mahdieh

1

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27 June 2017

Bahareh Rabbani

series ordinal

2

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27 June 2017

publication date

1 January 2009

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International Journal of Audiology

27 June 2017

number of pages

8

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based on heuristic

inferred from page(s)

published in

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27 June 2017

volume

48

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27 June 2017

issue

6

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27 June 2017

page(s)

363-370

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Prevalent connexin 26 gene (GJB2) mutations in Japanese

27 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

Pediatric otolaryngologists' use of genetic testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant

21 January 2018

1 reference

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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/10.1080%2F14992020802607449

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

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

GJB2 mutations in the Swiss hearing impaired.

21 January 2018

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

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

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

A deafness-associated mutant human connexin 26 improves the epithelial barrier in vitro

21 January 2018

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https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Relevance of connexin deafness (DFNB1) to human evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Connexin26 mutations associated with nonsyndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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/10.1080%2F14992020802607449

Determination of the frequency of the 35delG allele in Brazilian neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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/10.1080%2F14992020802607449

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/10.1080%2F14992020802607449

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14992020802607449

10.1080/14992020802607449

21 January 2018

Identifiers

DOI

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27 June 2017

1 reference