Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations.
Tajsharghi H; Hilton-Jones D; Raheem O; Saukkonen AM; Oldfors A; Udd B; Brain: A Journal Of Neurology, 2010, vol. 133, issue Pt 5, p 1451, ISSN 14602156. ISBN 14602156.

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