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Q33957091-9485B1F6-DA97-4718-95D3-F1C26BCCACD4
Q33957091-9485B1F6-DA97-4718-95D3-F1C26BCCACD4
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http://www.wikidata.org/entity/statement/Q33957091-9485B1F6-DA97-4718-95D3-F1C26BCCACD4
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy
P2860
Q33957091-9485B1F6-DA97-4718-95D3-F1C26BCCACD4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33957091-9485B1F6-DA97-4718-95D3-F1C26BCCACD4
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wasDerivedFrom
816461f1e8eb58bf9721cb25600d22810504115a
P2860
Mutations in TPM3 are a common cause of congenital fiber type disproportion.