(Q39290447)

10 September 2017

title

GJB2 mutations in Baluchi population (English)

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10 September 2017

8

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10 September 2017

Anoosh Naghavi

1

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Carla Nishimura

2

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Kimia Kahrizi

3

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Yasser Riazalhosseini

4

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Niloofar Bazazzadegan

5

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Marzieh Mohseni

6

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Richard J H Smith

7

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10 September 2017

publication date

1 August 2008

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10 September 2017

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10 September 2017

volume

87

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issue

2

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page(s)

195-197

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https://scigraph.springernature.com/pub.10.1007/s12041-008-0031-5

10 September 2017

exact match

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cites work

GJB2 mutations: passage through Iran

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular epidemiology of DFNB1 deafness in France

1 reference

12 December 2020

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

1 reference

12 December 2020

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

1 reference

12 December 2020

The genetics of deafness

1 reference

12 December 2020

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.

1 reference

12 December 2020

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

1 reference

12 December 2020

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

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12 December 2020

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

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12 December 2020

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

1 reference

12 December 2020

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India

1 reference

12 December 2020

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss.

1 reference

12 December 2020

A genotype-phenotype correlation for GJB2 (connexin 26) deafness

1 reference

12 December 2020

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.

1 reference

12 December 2020

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S12041-008-0031-5

Identifiers

DOI

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release_znalhxhbv5cdffod2ko4g6potq

10 September 2017

Fatcat ID

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