Open AccessA Novel Mutation in the GJB2 (Connexin 26) Gene in Egyptian Children with Non-syndromic Sensorineural Hearing Loss
Author(s) -
Nagwa A. Meguid,
Motaza H. Omran,
Iman A. Ghorab,
Ahmed A. Dardir,
Ehab Ragaa,
Suzette I. Helal,
Mona Anwar
Publication year - 2013
Publication title -
macedonian journal of medical sciences
Language(s) - English
Resource type - Journals
eISSN - 1857-5773
pISSN - 1857-5749
DOI - 10.3889/mjms.1857-5773.2013.0287
Subject(s) - medicine , connexin , sensorineural hearing loss , hearing loss , mutation , genetics , gene , audiology , gap junction , biology , intracellular