Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations
Author:   Sharif Fadel ,  Essammak Badria
Publisher:   LAP Lambert Academic Publishing
ISBN:  

9783659803796


Pages:   72
Publication Date:   12 November 2015
Format:   Paperback
Availability:   In stock   Availability explained
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Non-Syndromic Autosomal Recessive Deafness due to GJB2 Gene Mutations


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Overview

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.

Full Product Details

Author:   Sharif Fadel ,  Essammak Badria
Publisher:   LAP Lambert Academic Publishing
Imprint:   LAP Lambert Academic Publishing
Dimensions:   Width: 15.20cm , Height: 0.40cm , Length: 22.90cm
Weight:   0.118kg
ISBN:  

9783659803796


ISBN 10:   3659803790
Pages:   72
Publication Date:   12 November 2015
Audience:   General/trade ,  General
Format:   Paperback
Publisher's Status:   Active
Availability:   In stock   Availability explained
We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately.

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