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G.O.2: Mutations in LMOD3 cause severe nemaline myopathy by disrupting thin filament organisation in skeletal muscle

Bibliographic reference Kreissl, M. ; Sandaradura, S.A. ; Dowling, J.J. ; Kostyukova, A.S. ; Moroz, N. ; et. al. G.O.2: Mutations in LMOD3 cause severe nemaline myopathy by disrupting thin filament organisation in skeletal muscle. In: Neuromuscular Disorders, Vol. 24, no. 9-10, p. 792-793 (2014)
Permanent URL http://hdl.handle.net/2078.1/150754