GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent-Reference-Cited by-同舟云学术

GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent

Published:2010-06 Issue:6 Volume:74 Page:611-618
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Shan Jidong,Chobot-Rodd Janie,Castellanos Raquel,Babcock Melanie,Shanske Alan,Parikh Sanjay R.,Morrow Bernice E.,Samanich Joy

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference35 articles.

1. Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment;Samanich;Am. J. Med. Genet. A,2007

2. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population;Marazita;Am. J. Med. Genet.,1993

3. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus;Van Camp;J. Med. Genet.,1999

4. Genetic causes of hearing loss;Willems;N. Engl. J. Med.,2000

5. A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy;Rodriguez-Ballesteros;Hum. Mutat.,2008

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