Literature DB >> 26275501

Genetics of Hearing Loss--Nonsyndromic.

Kay W Chang1.   

Abstract

Eighty percent of nonsyndromic hearing losses are caused by autosomal-recessive (AR) inheritance, while most of the other 20% are caused by autosomal-dominant (AD) inheritance. Although AR nonsyndromic SNHL is most commonly caused by GJB2 and SLC26A4, there is no single gene that accounts for any significant proportion of AD SNHL. High-throughput sequencing techniques, also called next-generation sequencing (NGS) or massively parallel sequencing (MPS), may allow for routine definitive diagnosis of all possible genetic causes for hearing loss in the not-too-distant future.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  DFNA; DFNB; GJB2; Massively parallel sequencing; Next-generation sequencing; Nonsyndromic hearing loss

Mesh:

Substances:

Year:  2015        PMID: 26275501     DOI: 10.1016/j.otc.2015.06.005

Source DB:  PubMed          Journal:  Otolaryngol Clin North Am        ISSN: 0030-6665            Impact factor:   3.346


  13 in total

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