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Q39008908-FF6513DD-BF79-4C5E-9983-2F64D854950D
Q39008908-FF6513DD-BF79-4C5E-9983-2F64D854950D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39008908-FF6513DD-BF79-4C5E-9983-2F64D854950D
RYR1-related myopathies: a wide spectrum of phenotypes throughout life.
P2860
Q39008908-FF6513DD-BF79-4C5E-9983-2F64D854950D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39008908-FF6513DD-BF79-4C5E-9983-2F64D854950D
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wasDerivedFrom
59029ed44a69f24e38b1e5e862cb79e915c1b1c8
P2860
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.