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"Myopathy," myosin storage
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov CONGENITAL MYOPATHY 7A, MYOSIN STORAGE, AUTOSOMAL DOMINANT; CMYP7A PubMed Armel TZ, Leinwand LA. ...
- ... mutations in the MYH7 gene are involved in myosin storage myopathy. This condition causes muscle weakness and is characterized ... muscle fibers. The MYH7 gene mutations that cause myosin storage myopathy change amino acids in the tail region of ...
- ... MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy. Neuromuscul Disord. 2011 Apr;21(4):254-62. ...