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Q24675329-0487F21D-6437-4917-933F-1DBB91500568
Q24675329-0487F21D-6437-4917-933F-1DBB91500568
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http://www.wikidata.org/entity/statement/Q24675329-0487F21D-6437-4917-933F-1DBB91500568
Central core disease: clinical, pathological, and genetic features
P2860
Q24675329-0487F21D-6437-4917-933F-1DBB91500568
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24675329-0487F21D-6437-4917-933F-1DBB91500568
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wasDerivedFrom
c025aa5aabfa98e6b073c29d3fa9282792c11fc9
P2860
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.