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

✍ Scribed by 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


Book ID
116794898
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
48 KB
Volume
21
Category
Article
ISSN
0960-8966

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