Characterization of Vestibular Dysfunction in the Mouse Model for Usher Syndrome 1F-Reference-Cited by-同舟云学术

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Characterization of Vestibular Dysfunction in the Mouse Model for Usher Syndrome 1F

Published:2005-06 Issue:2 Volume:6 Page:106-118
ISSN:1525-3961
Container-title:Journal of the Association for Research in Otolaryngology
language:en
Short-container-title:JARO

Author:

Alagramam Kumar N.,Stahl John S.,Jones Sherri M.,Pawlowski Karen S.,Wright Charles G.

Publisher

Springer Science and Business Media LLC

Subject

Sensory Systems,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s10162-004-5032-3.pdf

Reference31 articles.

1. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

2. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

3. A New Mouse Insertional Mutation That Causes Sensorineural Deafness and Vestibular Defects

4. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

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