MYH2

Publications

Tajsharghi H, Oldfors A. Myosinopathies: pathology and mechanisms. Acta Neuropathol, 2013;125(1):3-18, PMID: 22918376.

Tajsharghi H et al. Human disease caused by loss of fast IIa myosin heavy chain due to recessive MYH2 mutations. Brain. 2010;133(Pt 5):1451-9. doi: 10.1093/brain/awq083. PMID: 20418530.