Open AccessP. [V27i; E114g] Compound Heterozygous State in Gjb2 Gene Could Be an Indicator of the Severity of Congenital Hearing Loss
Author(s) -
Tufan T Erkoc,
Yilmaz MB Comertpay G
Publication year - 2015
Publication title -
otolaryngology
Language(s) - English
Resource type - Journals
ISSN - 2161-119X
DOI - 10.4172/2161-119x.1000209
Subject(s) - compound heterozygosity , loss of heterozygosity , hearing loss , missense mutation , genetics , exon , gene , biology , mutation , congenital hearing loss , medicine , allele , audiology , sensorineural hearing loss