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P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis
P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis
2011
M. Vorgerd
Rudolf A. Kley
Piraye Serdaroglu-Oflazer
Zagaa Odgerel
Montse Olivé
Hee-Suk Lee
Y. Hahn
P.F.M. van der Ven
Jörg Höhfeld
Janbernd Kirschner
Juan M. Bilbao
Lev G. Goldfarb
Dieter O. Fürst
Keywords:
Biology
Genetics
Pathogenesis
Phenotype
Filamin
Myofibrillar myopathy
Correction
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