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Q30343979-5DD42669-77DD-4F88-ADB5-6E8DFFADF49F
Q30343979-5DD42669-77DD-4F88-ADB5-6E8DFFADF49F
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Statement
http://www.wikidata.org/entity/statement/Q30343979-5DD42669-77DD-4F88-ADB5-6E8DFFADF49F
Congenital myopathies: diseases of the actin cytoskeleton.
P2860
Q30343979-5DD42669-77DD-4F88-ADB5-6E8DFFADF49F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30343979-5DD42669-77DD-4F88-ADB5-6E8DFFADF49F
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wasDerivedFrom
ff1218d59e03ed7855a512107db08597babe67c3
P2860
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.