(Q50487258)

14 March 2018

title

Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss. (English)

1 reference

14 March 2018

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1 reference

L Bason

1

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14 March 2018

T Dudley

2

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14 March 2018

K Lewis

3

1 reference

14 March 2018

U Shah

4

1 reference

14 March 2018

W Potsic

5

1 reference

14 March 2018

A Ferraris

6

1 reference

14 March 2018

P Fortina

7

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14 March 2018

E Rappaport

8

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14 March 2018

I D Krantz

9

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14 March 2018

publication date

1 June 2002

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14 March 2018

published in

Clinical Genetics

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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)

459-464

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14 March 2018

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

1 reference

Genetic epidemiology of hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

Prevalent connexin 26 gene (GJB2) mutations in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

Connexin 26 studies in patients with sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

Connexin 26 Gene Mutations in Congenitally Deaf Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610611.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2002.610611.X

1 reference

14 March 2018

1 reference

14 March 2018