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Q28508101-5FB3851F-F4A2-4A39-B447-DAFDD1AB0A20
Q28508101-5FB3851F-F4A2-4A39-B447-DAFDD1AB0A20
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http://www.wikidata.org/entity/statement/Q28508101-5FB3851F-F4A2-4A39-B447-DAFDD1AB0A20
The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease
P2860
Q28508101-5FB3851F-F4A2-4A39-B447-DAFDD1AB0A20
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28508101-5FB3851F-F4A2-4A39-B447-DAFDD1AB0A20
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wasDerivedFrom
323e6d582aca714df70634fdd2364b2e0f32f65a
P2860
Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.