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Mutation Associated with an Autosomal Dominant Cone-Rod Dystrophy CORD7 Modifies RIM1-Mediated Modulation of Voltage-Dependent Ca2+ Channels
It is demonstrated here that the mouse RIM1 arginine‑to‑histidine substitution (R655H), which corresponds to the human CORD7 mutation, modifies RIM 1 function in regulating VDCC currents elicited by the P/Q‑ type Cav2.1 and L‑type Cav1.4 channels.