Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations 1

Vetenskap & teknik

Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations

Sharif Fadel • Essammak Badria

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72 sidor
2015

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+1G>A, 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.

Författare: Sharif Fadel, Essammak Badria
Format: Pocket/Paperback
ISBN: 9783659803796
Språk: Engelska
Antal sidor: 72
Utgivningsdatum: 2015-11-12
Förlag: LAP Lambert Academic Publishing