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Q28284668-AC9C94F6-F7FF-4B7F-B1C5-F295C80A27BA
Q28284668-AC9C94F6-F7FF-4B7F-B1C5-F295C80A27BA
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http://www.wikidata.org/entity/statement/Q28284668-AC9C94F6-F7FF-4B7F-B1C5-F295C80A27BA
Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects
P2860
Q28284668-AC9C94F6-F7FF-4B7F-B1C5-F295C80A27BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284668-AC9C94F6-F7FF-4B7F-B1C5-F295C80A27BA
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wasDerivedFrom
8aa5966f7eec3140f3e225c6e7b7f347ee863019
P2860
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4