Open AccessDetection of 35delG, 167delT mutations in the connexin 26 gene among Egyptian patients with nonsyndromic sensorineural hearing loss
Author(s) -
Nehal E. El Barbary,
Mervat F. El Belbesy,
Samir Asal,
Soha Kholeif
Publication year - 2015
Publication title -
the egyptian journal of otolaryngology
Language(s) - English
Resource type - Journals
eISSN - 2090-8539
pISSN - 1012-5574
DOI - 10.4103/1012-5574.152707
Subject(s) - medicine , hearing loss , heterozygote advantage , sensorineural hearing loss , compound heterozygosity , allele , genetics , mutation , connexin , audiology , genetic counseling , genetic testing , population , gene , biology , environmental health , intracellular , gap junction
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