Audiometric, Vestibular, and Genetic Aspects of a DFNA9 Family with a G88E COCH Mutation-Reference-Cited by-同舟云学术

Audiometric, Vestibular, and Genetic Aspects of a DFNA9 Family with a G88E COCH Mutation

Published:2005-09 Issue:5 Volume:26 Page:926-933
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Kemperman Martijn H,De Leenheer Els M. R,Huygen Patrick L. M,van Duijnhoven Gerard,Morton Cynthia C,Robertson Nahid G,Cremers Frans P. M,Kremer Hannie,Cremers Cor W. R. J

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference27 articles.

1. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.;Manolis;Hum Mol Genet,1996

2. Clinical presentation of DFNA11 (MYO7A).;Tamagawa;Adv Otorhinolaryngol,2002

3. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.;Robertson;Nat Genet,1998

4. Mapping and characterization of a novel cochlear gene in human and in mouse: A positional candidate gene for a deafness disorder, DFNA9.;Robertson;Genomics,1997

5. Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin.;Grabski;Hum Genet,2003

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