Tmprss3, a Transmembrane Serine Protease Deficient in Human DFNB8/10 Deafness, Is Critical for Cochlear Hair Cell Survival at the Onset of Hearing

Mutations in the type II transmembrane serine protease 3 (TMPRSS3) gene cause non-syndromic autosomal recessive deafness (DFNB8/10), characterized by congenital or childhood onset bilateral profound hearing loss. In order to explore the physiopathology of TMPRSS3 related deafness, we have generated...

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Detalhes bibliográficos
Main Authors: Fasquelle, Lydie, Scott, Hamish S., Lenoir, Marc, Wang, Jing, Rebillard, Guy, Gaboyard, Sophie, Venteo, Stéphanie, François, Florence, Mausset-Bonnefont, Anne-Laure, Antonarakis, Stylianos E., Neidhart, Elizabeth, Chabbert, Christian, Puel, Jean-Luc, Guipponi, Michel, Delprat, Benjamin
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2011
Assuntos:
Molecular Bases of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3089580/
https://ncbi.nlm.nih.gov/pubmed/21454591
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.190652
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