P5.56 Myofibrillar myopathy associated with filamin C...

Neuromuscular Disorders 2011 Vol. 21; Iss. 9-10

P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis

M. Vorgerd, R.A. Kley, P. Serdaroglu-Oflazer, Z. Odgerel, M. Olive, H.S. Lee, Y. Hahn, P.F.M. van der Ven, J. Höhfeld, J. Kirschner, J.M. Bilbao, L.G. Goldfarb, D.O. Fürst
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.1085
File:
PDF, 48 KB
english, 2011
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