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Q36188563-2640114D-620B-4045-88A8-6393E1F5491B
Q36188563-2640114D-620B-4045-88A8-6393E1F5491B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36188563-2640114D-620B-4045-88A8-6393E1F5491B
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.
P2860
Q36188563-2640114D-620B-4045-88A8-6393E1F5491B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36188563-2640114D-620B-4045-88A8-6393E1F5491B
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wasDerivedFrom
825330a3dd5ecf35453d9e736986f14c885fe493
P2860
A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy