Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation†

Usher syndrome 3A (USH3A) is an autosomal recessive disorder characterized by progressive loss of hearing and vision due to mutation in the clarin-1 (CLRN1) gene. Lack of an animal model has hindered our ability to understand the function of CLRN1 and the pathophysiology associated with USH3A. Here...

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Main Authors: Geng, Ruishuang, Geller, Scott F., Hayashi, Toshinori, Ray, Catherine A., Reh, Thomas A., Bermingham-McDonogh, Olivia, Jones, Sherri M., Wright, Charles G., Melki, Sami, Imanishi, Yoshikazu, Palczewski, Krzysztof, Alagramam, Kumar N., Flannery, John G.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2009
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2706682/
https://ncbi.nlm.nih.gov/pubmed/19414487
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp210
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