Mutation associated with an autosomal dominant cone-rod dystrophy CORD7 modifies RIM1-mediated modulation of voltage-dependent Ca2+ channels

Genetic analyses have revealed an association of the gene encoding the Rab3A-interacting molecule (RIM1) with an autosomal dominant cone-rod dystrophy CORD7. However, the pathogenesis of CORD7 has remained unclear. Recently, we have revealed that RIM1 exerts functional impacts on voltage-dependent C...

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Publicado no:Channels (Austin)
Main Authors: Miki, Takafumi, Kiyonaka, Shigeki, Uriu, Yoshitsugu, De Waard, Michel, Wakamori, Minoru, Beedle, Aaron, Campbell, Kevin, Mori, Yasuo
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4850211/
https://ncbi.nlm.nih.gov/pubmed/18690027
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