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Q34545457-71A6DB2F-6A9F-4A3B-8B84-FA03D4E653BA
Q34545457-71A6DB2F-6A9F-4A3B-8B84-FA03D4E653BA
BestRank
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http://www.wikidata.org/entity/statement/Q34545457-71A6DB2F-6A9F-4A3B-8B84-FA03D4E653BA
Ca2+ release in muscle fibers expressing R4892W and G4896V type 1 ryanodine receptor disease mutants
P2860
Q34545457-71A6DB2F-6A9F-4A3B-8B84-FA03D4E653BA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34545457-71A6DB2F-6A9F-4A3B-8B84-FA03D4E653BA
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wasDerivedFrom
b76da5579b8928cc87f7c6ad04cc616b34fcdac1
P2860
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.