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Q36188563-73B9552B-6283-48CE-BF8E-3EB5652FF4E6
Q36188563-73B9552B-6283-48CE-BF8E-3EB5652FF4E6
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http://www.wikidata.org/entity/statement/Q36188563-73B9552B-6283-48CE-BF8E-3EB5652FF4E6
Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.
P2860
Q36188563-73B9552B-6283-48CE-BF8E-3EB5652FF4E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36188563-73B9552B-6283-48CE-BF8E-3EB5652FF4E6
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wasDerivedFrom
825330a3dd5ecf35453d9e736986f14c885fe493
P2860
Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.