High-throughput screening for GJB2 mutations—its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations-Reference-Cited by-同舟云学术

High-throughput screening for GJB2 mutations—its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations

Published:2002-07 Issue:3 Volume:29 Page:231-239
ISSN:0385-8146
Container-title:Auris Nasus Larynx
language:en
Short-container-title:Auris Nasus Larynx

Author:

Sugata Akemi,Fukushima Kunihiro,Sugata Ken-ichi,Fukuda Syouichiro,Kimura Nobuhiko,Gunduz Mehmet,Kasai Norio,Usami Shinichi,Smith Richard J.H,Nishizaki Kazunori

Publisher

Elsevier BV

Subject

General Medicine,Otorhinolaryngology,Surgery

Reference24 articles.

1. Genetic epidemiology of hearing impairment;Morton;Ann. NY Acad. Sci.,1991

2. MYO1F as a candidate gene for nonsyndromic deafness, DFNB15;Chen;Arch. Otolaryngol. Head Neck Surg.,2001

3. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q;Guilford;Nat. Genet.,1994

4. The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population;Maw;Am. J. Hum. Genet.,1995

5. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene;Rabionet;Hum. Genet.,2000

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