Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India-Reference-Cited by-同舟云学术

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Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India

Published:2015-12 Issue:2 Volume:573 Page:239-245
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Adhikary Bidisha,Ghosh Sudakshina,Paul Silpita,Bankura Biswabandhu,Pattanayak Arup Kumar,Biswas Subhradev,Maity Biswanath,Das Madhusudan

Funder

Department of Biotechnology, Govt. of West Bengal, India

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference46 articles.

1. Spectrum of GJB2 mutations causing deafness in the British Bangladeshi population;Bajaj;Clin. Otolaryngol.,2008

2. Ethnic India: a genomic view, with special reference to peopling and structure;Basu;Genome Res.,2003

3. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in north Indian patients with non-syndromic hearing impairment;Bhalla;Biochem. Biophys. Res. Commun.,2009

4. Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness;Bruzzone;FEBS Lett.,2003

5. A genotype–phenotype correlation for GJB2 (connexin 26) deafness;Cryns;J. Med. Genet.,2004

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1. Building genomic capacity for precision health in Africa;Nature Medicine;2024-07

2. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China;BMC Medical Genomics;2024-02-20

3. Identification of novel gene variants causing autosomal recessive non-syndromic hearing loss in Iranian families;2024-02-20

4. A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing Impairment;Indian Journal of Otolaryngology and Head & Neck Surgery;2023-07-07

5. GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal;Biology;2022-05-23

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