A small molecule mitigates hearing loss in a mouse model of Usher syndrome III

Usher syndrome type III (USH3) characterized by progressive deafness, variable balance disorder, and blindness is caused by destabilizing mutations in the gene encoding the clarin-1 protein (CLRN1). Here we report a novel strategy to mitigate hearing loss associated with a common USH3 mutation CLRN1...

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Detalles Bibliográficos
Autores principales: Alagramam, Kumar N., Gopal, Suhasini R., Geng, Ruishuang, Chen, Daniel H.-C., Nemet, Ina, Lee, Richard, Tian, Guilian, Miyagi, Masaru, Malagu, Karine F., Lock, Christopher J., Esmieu, William R. K., Owens, Andrew P., Lindsay, Nicola A., Ouwehand, Krista, Albertus, Faywell, Fischer, David F., Bürli, Roland W., MacLeod, Angus M., Harte, William E., Palczewski, Krzysztof, Imanishi, Yoshikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871731/
https://www.ncbi.nlm.nih.gov/pubmed/27110679
http://dx.doi.org/10.1038/nchembio.2069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871731/
https://www.ncbi.nlm.nih.gov/pubmed/27110679
http://dx.doi.org/10.1038/nchembio.2069

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