Spectrum of GJB2 Mutations in a Cohort of Nonsyndromic Hearing Loss Cases from the Kingdom of Saudi Arabia-Reference-Cited by-同舟云学术

Spectrum of GJB2 Mutations in a Cohort of Nonsyndromic Hearing Loss Cases from the Kingdom of Saudi Arabia

Published:2010-02 Issue:1 Volume:14 Page:79-83
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Al-Qahtani Mohammed H.¹,Baghlab Ibtessam¹,Chaudhary Adeel G.¹,Abuzenadah Adel M.¹,Bamanie Afaf²,Daghistani Kamal J.³,Safieh Malek⁴,Fida Loai⁵,Dallol Ashraf¹

Affiliation:

1. Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

2. Audiology Section, Department of Otolaryngology, KAUH, Jeddah, Kingdom of Saudi Arabia.

3. Ear, Nose, Throat (ENT)—Head and Neck Surgery Department, Erfan-Bagedo Hospital, Jeddah, Kingdom of Saudi Arabia.

4. Jeddah Institute for Speech and Hearing, Jeddah, Kingdom of Saudi Arabia.

5. Medical Supervision, Department of Education, Jeddah, Kingdom of Saudi Arabia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2009.0111

Reference30 articles.

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

2. Carrier Rates of the Ancestral Indian W24X Mutation in GJB2 in the General Gypsy Population and Individual Subisolates

3. Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa

4. Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

5. A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

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