P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis
| Autor: | Vorgerd, M., Kley, R.A., Serdaroglu-Oflazer, P., Odgerel, Z., Olive, M., Lee, H.S., Hahn, Y., van der Ven, P.F.M., Höhfeld, J., Kirschner, J., Bilbao, J.M., Goldfarb, L.G., Fürst, D.O. |
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| Zdroj: | In Neuromuscular Disorders October 2011 21(9-10):741-741 |
| Databáze: | ScienceDirect |
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