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Q37458493-0EBBCF9B-A90F-47E4-B0D1-B488FEC9F948
Q37458493-0EBBCF9B-A90F-47E4-B0D1-B488FEC9F948
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-0EBBCF9B-A90F-47E4-B0D1-B488FEC9F948
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P921
Q37458493-0EBBCF9B-A90F-47E4-B0D1-B488FEC9F948
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-0EBBCF9B-A90F-47E4-B0D1-B488FEC9F948
rank
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type
BestRank
Statement
P921
birth defect