Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations

Name: Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations
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Description

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.

Release date NZ

November 12th, 2015

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General (US: Trade)

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152x229x4

ISBN-13

9783659803796

Product ID

24523092

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Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations

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