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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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| Udgivet i: | Channels (Austin) |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Landes Bioscience
2007
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4850211/ https://ncbi.nlm.nih.gov/pubmed/18690027 |
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