Molecular genetics of non-syndromic deafness.

Abstract:

:One in every 1,000 newborn suffers from congenital hearing impairment. More than 60% of the congenital cases are caused by genetic factors. In most cases, hearing loss is a multifactorial disorder caused by both genetic and environmental factors. Molecular genetics of deafness has experienced remarkable progress in the last decade. Genes responsible for hereditary hearing impairment are being mapped and cloned progressively. This review focuses on non-syndromic hearing loss, since the gene involved in this type of hearing loss have only recently begun to be identified.

authors

Piatto VB,Nascimento EC,Alexandrino F,Oliveira CA,Lopes AC,Sartorato EL,Maniglia JV

doi

10.1016/s1808-8694(15)31313-6

subject

Has Abstract

pub_date

2005-03-01 00:00:00

pages

216-23

issue

2

eissn

1808-8694

issn

1808-8686

pii

S1808-8694(15)31313-6

journal_volume

71

pub_type

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