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Q28284847-6E8E2B74-E3BF-4D6F-B0B2-A2B707E2DEB3
Q28284847-6E8E2B74-E3BF-4D6F-B0B2-A2B707E2DEB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284847-6E8E2B74-E3BF-4D6F-B0B2-A2B707E2DEB3
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity
P1433
Q28284847-6E8E2B74-E3BF-4D6F-B0B2-A2B707E2DEB3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28284847-6E8E2B74-E3BF-4D6F-B0B2-A2B707E2DEB3
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type
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P1433
Brain