Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations.
Tajsharghi, Homa; Hilton-Jones, David; Raheem, Olayinka; Saukkonen, Anna Maija; Oldfors, Anders; Udd, Bjarne; Brain: A Journal of Neurology, 2010, vol. 133, issue 5, p 1451, ISSN 00068950. ISBN 14602156.

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