Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations - Sharif, Fadel;Essammak, Badria
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The ubiquity of GJB2-associated hearing loss around the world is notable for a highly prevalent genetic disease. This work confirms the significant contribution of GJB2 gene mutations, particularly c.35delG, c.235delC and c.-23+1GA, to congenital hearing loss in Gaza strip children and serves as both a reference for clinicians working up and counseling. Patients with congenital autosomal recessive non-syndromic hearing loss.

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Produktbeschreibung
The ubiquity of GJB2-associated hearing loss around the world is notable for a highly prevalent genetic disease. This work confirms the significant contribution of GJB2 gene mutations, particularly c.35delG, c.235delC and c.-23+1GA, to congenital hearing loss in Gaza strip children and serves as both a reference for clinicians working up and counseling. Patients with congenital autosomal recessive non-syndromic hearing loss.
Autorenporträt
Dr. Fadel A. Sharif is a Molecular Biology professor at the Islamic University of Gaza (IUG) where he serves as the Director of the Genetic Diagnosis Unit. He is an expert in Genetics and Molecular Biology, which are the subjects he teaches and researches at IUG. He is the author of many scientific publications.