Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations
Tajsharghi, H. ; Hilton-Jones, D. ; Raheem, O. ; Saukkonen, A. M. ; Oldfors, A. ; Udd, B.; Brain, 2010, vol. 133, issue 5, p 1451, ISSN 00068950. ISBN 14602156.

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