Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing-Reference-Cited by-同舟云学术

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Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

Published:2015-02-15 Issue:3 Volume:3 Page:189-196
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Ammar‐Khodja Fatima¹,Bonnet Crystel²,Dahmani Malika¹,Ouhab Sofiane³,Lefèvre Gaelle M.²,Ibrahim Hassina⁴,Hardelin Jean‐Pierre⁵,Weil Dominique⁵,Louha Malek⁶,Petit Christine²⁵⁷

Affiliation:

1. Equipe de Génétique, Laboratoire de Biologie Moléculaire Faculté des Sciences Biologiques Université des Sciences et de la Technologie Houari Boumédiène (USTHB) Alger Algeria

2. Institut de la Vision UMRS 1120 INSERM/UPMC/Institut Pasteur Paris France

3. Service d'Otorhinolaryngologie (ORL) Hôpital de Kouba‐Bachir Mentouri Alger Algeria

4. Service d'Otorhinolaryngologie (ORL) Hôpital Mustapha Pacha Alger Algeria

5. Institut Pasteur Unité de Génétique et Physiologie de l'Audition UMRS 1120 INSERM/UPMC Paris 6 Paris France

6. Service de Biochimie Hôpital Armand Trousseau UMRS 1120 INSERM Paris France

7. Collège de France Paris France

Funder

Ministère de l'Enseignement Supérieur et de la Recherche Scientifique, Gouvernement de la République Algérienne

BNP PARIBAS

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.131

Reference51 articles.

1. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

2. The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3

3. Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F

4. Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss

5. Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

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