The familial hemiplegic migraine mutation R192q reduces G‐protein‐mediated inhibition of p/q‐type (Ca v 2.1) calcium channels expressed in human embryonic kidney cells
Author:
Affiliation:
1. Merck Sharp and Dohme Research Laboratories, The Neuroscience Research Centre, Terlings Park, Eastwick Road, Harlow, Essex CM20 2QR, UK
2. Department of Biochemical Pharmacology, University of Innsbruck, A‐6020 Innsbruck, Austria
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/jphysiol.2002.026716
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1. Voltage-Gated Ion Channels and Electrical Excitability
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4. A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia
5. Neurotransmitter inhibition of neuronal calcium currents by changes in channel voltage dependence
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