(Q50457500)

14 March 2018

title

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population. (English)

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14 March 2018

author name string

Pu Dai

1

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14 March 2018

Fei Yu

2

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14 March 2018

Bing Han

3

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14 March 2018

Yongyi Yuan

4

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14 March 2018

Qi Li

5

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14 March 2018

Guojian Wang

6

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14 March 2018

Xin Liu

7

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14 March 2018

Jia He

8

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14 March 2018

Deliang Huang

9

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14 March 2018

Dongyang Kang

10

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14 March 2018

Xin Zhang

11

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14 March 2018

Huijun Yuan

12

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14 March 2018

Eric Schmitt

13

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14 March 2018

Dongyi Han

14

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14 March 2018

Lee-Jun Wong

15

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14 March 2018

language of work or name

English

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publication date

1 May 2007

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14 March 2018

published in

Genetics in Medicine

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14 March 2018

volume

9

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14 March 2018

issue

5

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14 March 2018

page(s)

283-289

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14 March 2018

https://scigraph.springernature.com/pub.10.1097/gim.0b013e31804d2371

exact match

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cites work

Hereditary deafness and phenotyping in humans

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Connexin26 mutations associated with nonsyndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Prevalent connexin 26 gene (GJB2) mutations in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Molecular epidemiology of DFNB1 deafness in France

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

GJB2 mutations and degree of hearing loss: a multicenter study

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

Population structure and history in East Asia

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E31804D2371

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/10.1097%2FGIM.0B013E31804D2371

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

21 January 2018

1 reference

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10.1097/GIM.0B013E31804D2371

21 January 2018

Identifiers

DOI

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14 March 2018

Dimensions Publication ID

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14 March 2018