Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss
Author:
Funder
University of Tübingen
NIH/COBRE
Presbyterian Health Foundation
Publisher
Elsevier BV
Subject
Sensory Systems
Reference258 articles.
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3. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC;Ahmed;Hum. Genet.,2002
4. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23;Ahmed;Hum. Mol. Genet.,2003
5. Mutations of MYO6 are associated with recessive deafness, DFNB37;Ahmed;Am. J. Hum. Genet.,2003
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