Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene (GJB2) in the Moroccan Population-Reference-Cited by-同舟云学术

Carrier Frequencies of Mutations/Polymorphisms in the Connexin 26 Gene (GJB2) in the Moroccan Population

Published:2008-12 Issue:4 Volume:12 Page:569-574
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Abidi Omar¹²,Boulouiz Redouane¹,Nahili Halima¹,Bakhouch Khadija³,Wakrim Lahcen³,Rouba Hassan¹,Chafik Abdelaziz²,Hassar Mohammed¹,Barakat Abdelhamid¹

Affiliation:

1. Laboratory of Human Genetics, Department of Scientific Research, Pasteur Institute, Casablanca, Morocco.

2. Laboratory of Anthropogenetic and Biostatistic Sciences, Department of Biology, Faculty of Sciences, University of Chouaib Doukkali, El Jadida, Morocco.

3. Laboratory of Virology, Department of Scientific Research, Pasteur Institute, Casablanca, Morocco.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2008.0063

Reference48 articles.

1. Prevalent connexin 26 gene (GJB2) mutations in Japanese

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

3. Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation

4. High carrier frequency of the GJB2 mutation (35delG) in the north of Iran

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4. A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family;International Journal of Pediatric Otorhinolaryngology;2016-08

5. Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss;European Journal of Medical Genetics;2016-06