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Q38119858-A586FC03-73B0-4B59-898F-A45530BC6CDF
Q38119858-A586FC03-73B0-4B59-898F-A45530BC6CDF
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http://www.wikidata.org/entity/statement/Q38119858-A586FC03-73B0-4B59-898F-A45530BC6CDF
Polymorphism in tropomyosin structure and function.
P2860
Q38119858-A586FC03-73B0-4B59-898F-A45530BC6CDF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38119858-A586FC03-73B0-4B59-898F-A45530BC6CDF
rank
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wasDerivedFrom
1e0a7cda7f317e3f1367097e91793e26ecbe07c4
P2860
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity