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Q36586052-2EFD3EB3-FB60-42E3-8D9C-33F6F82EAACE
Q36586052-2EFD3EB3-FB60-42E3-8D9C-33F6F82EAACE
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http://www.wikidata.org/entity/statement/Q36586052-2EFD3EB3-FB60-42E3-8D9C-33F6F82EAACE
Novel excitation-contraction uncoupled RYR1 mutations in patients with central core disease.
P2860
Q36586052-2EFD3EB3-FB60-42E3-8D9C-33F6F82EAACE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36586052-2EFD3EB3-FB60-42E3-8D9C-33F6F82EAACE
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wasDerivedFrom
c6fb2ed7b432fa902ab3827f6fa722b1190ea83c
P2860
Ca2+ dysregulation in Ryr1(I4895T/wt) mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods