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Q28284668-3CA514FE-36CD-4EE5-96F5-041E7CE4B22A
Q28284668-3CA514FE-36CD-4EE5-96F5-041E7CE4B22A
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http://www.wikidata.org/entity/statement/Q28284668-3CA514FE-36CD-4EE5-96F5-041E7CE4B22A
Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects
P2860
Q28284668-3CA514FE-36CD-4EE5-96F5-041E7CE4B22A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284668-3CA514FE-36CD-4EE5-96F5-041E7CE4B22A
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wasDerivedFrom
8aa5966f7eec3140f3e225c6e7b7f347ee863019
P2860
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.