Zebrafish Models for the Mechanosensory Hair Cell Dysfunction in Usher Syndrome 3 Reveal That Clarin-1 Is an Essential Hair Bundle Protein

Usher syndrome type III (USH3) is characterized by progressive loss of hearing and vision, and varying degrees of vestibular dysfunction. It is caused by mutations that affect the human clarin-1 protein (hCLRN1), a member of the tetraspanin protein family. The missense mutation CLRN1(N48K), which af...

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Publicado no:J Neurosci
Main Authors: Gopal, Suhasini R., Chen, Daniel H.-C., Chou, Shih-Wei, Zang, Jingjing, Neuhauss, Stephan C.F., Stepanyan, Ruben, McDermott, Brian M., Alagramam, Kumar N.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2015
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4502259/
https://ncbi.nlm.nih.gov/pubmed/26180195
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1096-15.2015
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