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Q37499827-21D5EA62-0E67-4AFE-8C1B-AD2A16A37A5E
Q37499827-21D5EA62-0E67-4AFE-8C1B-AD2A16A37A5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37499827-21D5EA62-0E67-4AFE-8C1B-AD2A16A37A5E
TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.
P2860
Q37499827-21D5EA62-0E67-4AFE-8C1B-AD2A16A37A5E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37499827-21D5EA62-0E67-4AFE-8C1B-AD2A16A37A5E
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wasDerivedFrom
47741729399675320444ed4bb580c66ecf9a2c65
P2860
Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.