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Q35673620-D2513973-A564-4929-8455-AB0E488DA405
Q35673620-D2513973-A564-4929-8455-AB0E488DA405
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35673620-D2513973-A564-4929-8455-AB0E488DA405
Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype.
P2860
Q35673620-D2513973-A564-4929-8455-AB0E488DA405
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35673620-D2513973-A564-4929-8455-AB0E488DA405
rank
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wasDerivedFrom
250760cfdc0949f398ff51593497e83d07f9f66c
P2860
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods