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Q47735755-2F2CED2E-F26D-41A2-8D88-B44768CC7FBC
Q47735755-2F2CED2E-F26D-41A2-8D88-B44768CC7FBC
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http://www.wikidata.org/entity/statement/Q47735755-2F2CED2E-F26D-41A2-8D88-B44768CC7FBC
Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).
P2860
Q47735755-2F2CED2E-F26D-41A2-8D88-B44768CC7FBC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47735755-2F2CED2E-F26D-41A2-8D88-B44768CC7FBC
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wasDerivedFrom
73f31602e7051a756acbbac8b21adbf2400383ba
P2860
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.