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Q36513343-406D51D9-2E8B-4E5C-86EB-1594D8791AC8
Q36513343-406D51D9-2E8B-4E5C-86EB-1594D8791AC8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36513343-406D51D9-2E8B-4E5C-86EB-1594D8791AC8
Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits.
P2860
Q36513343-406D51D9-2E8B-4E5C-86EB-1594D8791AC8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36513343-406D51D9-2E8B-4E5C-86EB-1594D8791AC8
rank
NormalRank
type
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Statement
wasDerivedFrom
d094470ee75b88b1588ebd5942ff57dfd22707ef
P2860
CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy