Spectrum and frequency ofGJB2mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients-Reference-Cited by-同舟云学术

Spectrum and frequency ofGJB2mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients

Published:2013-05-13 Issue:7 Volume:52 Page:466-471
ISSN:1499-2027
Container-title:International Journal of Audiology
language:en
Short-container-title:International Journal of Audiology

Author:

Matos Tiago Daniel,Simões-Teixeira Helena,Caria Helena,Gonçalves Ana Cláudia,Chora Joana,Correia Maria do Céu,Moura Carla,Rosa Helena,Monteiro Luísa,O’Neill Assunção,Dias Óscar,Andrea Mário,Fialho Graça

Publisher

Informa UK Limited

Subject

Speech and Hearing,Linguistics and Language,Language and Linguistics

Link

http://www.tandfonline.com/doi/pdf/10.3109/14992027.2013.783719

Reference39 articles.

1. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

2. Pathogenetic role of the deafness-related M34T mutation of Cx26

3. Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf

4. DFNB1-associated deafness in Portuguese cochlear implant users: Prevalence and impact on oral outcome

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