Mutations in the first MyTH4 domain ofMYO15Aare a common cause of DFNB3 hearing loss-Reference-Cited by-同舟云学术

Mutations in the first MyTH4 domain ofMYO15Aare a common cause of DFNB3 hearing loss

Published:2009-04 Issue:4 Volume:119 Page:727-733
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Shearer A. Eliot,Hildebrand Michael S.,Webster Jennifer A.,Kahrizi Kimia,Meyer Nicole C.,Jalalvand Khadijeh,Arzhanginy Sanaz,Kimberling William J.,Stephan Dietrich,Bahlo Melanie,Smith Richard J. H.,Najmabadi Hossein

Publisher

Wiley

Subject

Otorhinolaryngology

Reference20 articles.

1. Sensorineural hearing loss in children;Smith;Lancet,2005

2. Van Camp G, Smith RJH. Hereditary Hearing Loss Homepage. Available at: http://webh01.ua.ac.be/hhh/. Accessed June 17, 2008.

3. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17;Friedman;Nat Genet,1995

4. Association of unconventional myosin MYO15 mutations with human non-syndromic deafness DFNB3;Wang;Science,1998

5. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2;Liang;Genomics,1999

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