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[A heterozygous mutation, Arg1845Trp, in the distal rod region of slow myosin (type I, MYH7) is associated with familial congenital myopathy, with large deposits of MyHC I in the subsarcolemmal region of type 1 muscle fibres, `Myosin storage myopathy`.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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