Harmonin Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells-Reference-Cited by-同舟云学术

Harmonin Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells

Published:2009-05 Issue:3 Volume:62 Page:375-387
ISSN:0896-6273
Container-title:Neuron
language:en
Short-container-title:Neuron

Author:

Grillet Nicolas,Xiong Wei,Reynolds Anna,Kazmierczak Piotr,Sato Takashi,Lillo Concepcion,Dumont Rachel A.,Hintermann Edith,Sczaniecka Anna,Schwander Martin,Williams David,Kachar Bechara,Gillespie Peter G.,Müller Ulrich

Publisher

Elsevier BV

Subject

General Neuroscience

Reference46 articles.

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2. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F;Ahmed;Am. J. Hum. Genet.,2001

3. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC;Ahmed;Hum. Genet.,2002

4. The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15;Ahmed;J. Neurosci.,2006

5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene;Alagramam;Nat. Genet.,2001

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