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Using electrophysiology, cryo-EM, molecular simulations, and in vivo models, we also identify a druggable inhibitory site that could guide future therapies for cerebellar ataxia. (2/4)
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Structural snapshots capture an ataxia-linked overactive ion channel in its open state and reveal a druggable site for inhibition.
www.science.org
Functional and structural basis of a hypermorphic TRPC3 variant
Cordero-Vásquez Lab