(Q50487318)

14 March 2018

title

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

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14 March 2018

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Yi-Chun Wang

1

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14 March 2018

Chiu-Yun Kung

2

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14 March 2018

Mao-Chang Su

3

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14 March 2018

Ching-Chyuan Su

4

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14 March 2018

Hsiu-Mei Hsu

5

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14 March 2018

Chin-Chu Tsai

6

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14 March 2018

Chyi-Chyang Lin

7

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14 March 2018

Shuan-Yow Li

8

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14 March 2018

publication date

1 August 2002

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14 March 2018

European Journal of Human Genetics

published in

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14 March 2018

volume

10

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14 March 2018

issue

8

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14 March 2018

page(s)

495-498

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14 March 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200838

exact match

0 references

cites work

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

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/10.1038%2FSJ.EJHG.5200838

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/10.1038%2FSJ.EJHG.5200838

Ionic and potential changes of the endolymphatic sac induced by endolymph volume changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

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/10.1038%2FSJ.EJHG.5200838

Listening to silence and understanding nonsense: exonic mutations that affect splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

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/10.1038%2FSJ.EJHG.5200838

Functional analysis of human Cx26 mutations associated with deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

inferred from DOI database lookup

7 January 2021

based on heuristic

Connexin gene mutations in human genetic diseases.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200838

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5200838

1 reference

14 March 2018

1 reference

14 March 2018