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Q36460971-7F61F15F-848B-46A6-BA0C-D1828B052AA7
Q36460971-7F61F15F-848B-46A6-BA0C-D1828B052AA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-7F61F15F-848B-46A6-BA0C-D1828B052AA7
A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.
P5875
Q36460971-7F61F15F-848B-46A6-BA0C-D1828B052AA7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36460971-7F61F15F-848B-46A6-BA0C-D1828B052AA7
rank
NormalRank
type
BestRank
Statement
P5875
235615540
http://www.w3.org/2001/XMLSchema#string