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Q37458493-6AD9A2E8-C9DA-41F1-AD87-D4C88282B6B3
Q37458493-6AD9A2E8-C9DA-41F1-AD87-D4C88282B6B3
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http://www.wikidata.org/entity/statement/Q37458493-6AD9A2E8-C9DA-41F1-AD87-D4C88282B6B3
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods
P2860
Q37458493-6AD9A2E8-C9DA-41F1-AD87-D4C88282B6B3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37458493-6AD9A2E8-C9DA-41F1-AD87-D4C88282B6B3
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wasDerivedFrom
52b45f35f184e486ea9064cf422d36aaaf6bcf16
P2860
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.