Expression of Myh9 in the mammalian cochlea: Localization within the stereocilia
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference54 articles.
1. Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
2. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
3. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
4. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC
5. Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice
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