(Q50458112)

14 March 2018

title

GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection. (English)

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14 March 2018

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Shannon A Ross

1

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14 March 2018

Zdenek Novak

2

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14 March 2018

Rekha A Kumbla

3

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14 March 2018

Kui Zhang

4

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14 March 2018

Karen B Fowler

5

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14 March 2018

Suresh Boppana

6

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14 March 2018

language of work or name

English

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publication date

1 June 2007

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14 March 2018

published in

Pediatric Research

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14 March 2018

volume

61

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14 March 2018

issue

6

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14 March 2018

page(s)

687-691

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14 March 2018

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e3180536609

exact match

0 references

cites work

Symptomatic congenital cytomegalovirus. Disorders of language, learning, and hearing.

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Predictors of hearing loss in children with symptomatic congenital cytomegalovirus infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Cytomegalovirus urinary excretion and long term outcome in children with congenital cytomegalovirus infection. Congenital CMV Longitudinal Study Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Congenital cytomegalovirus infection: association between virus burden in infancy and hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Newborn hearing screening--a silent revolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Sensorineural hearing loss in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Neonatal screening for congenital cytomegalovirus infection by detection of virus in saliva

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Progressive and fluctuating sensorineural hearing loss in children with asymptomatic congenital cytomegalovirus infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

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/10.1203%2FPDR.0B013E3180536609

Pathogenetic role of the deafness-related M34T mutation of Cx26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

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/10.1203%2FPDR.0B013E3180536609

Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

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/10.1203%2FPDR.0B013E3180536609

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/10.1203%2FPDR.0B013E3180536609

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

HLA class II and TNF genes in African Americans from the Southeastern United States: regional differences in allele frequencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

Connexin-30 deletion analysis in connexin-26 heterozygotes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E3180536609

10.1203/PDR.0B013E3180536609

21 January 2018

Identifiers

DOI

1 reference

14 March 2018

Dimensions Publication ID

1034821492

0 references

1 reference

14 March 2018