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Q36513343-74C8863D-4D9E-41F2-AC0B-3F687D5532EC
Q36513343-74C8863D-4D9E-41F2-AC0B-3F687D5532EC
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Statement
http://www.wikidata.org/entity/statement/Q36513343-74C8863D-4D9E-41F2-AC0B-3F687D5532EC
Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits.
P2860
Q36513343-74C8863D-4D9E-41F2-AC0B-3F687D5532EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36513343-74C8863D-4D9E-41F2-AC0B-3F687D5532EC
rank
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wasDerivedFrom
d094470ee75b88b1588ebd5942ff57dfd22707ef
P2860
Absence epilepsy in tottering mutant mice is associated with calcium channel defects