(Q35433439)

8 August 2017

Prevalent connexin 26 gene (GJB2) mutations in Japanese (English)

1 reference

8 August 2017

S Abe

1

1 reference

8 August 2017

S Usami

2

1 reference

8 August 2017

H Shinkawa

3

1 reference

8 August 2017

P M Kelley

4

1 reference

8 August 2017

W J Kimberling

5

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 January 2000

1 reference

Journal of Medical Genetics

8 August 2017

1 reference

8 August 2017

37

1 reference

8 August 2017

1

1 reference

8 August 2017

41-43

1 reference

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

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

Connexin-26 mutations in sporadic and inherited sensorineural deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734448

26 September 2018

Identifiers

DOI

10.1136/JMG.37.1.41

1 reference

8 August 2017

1 reference

8 August 2017

1 reference