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

التفاصيل البيبلوغرافية
العنوان: P5.56 Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesis
المؤلفون: Lev G. Goldfarb, P.F.M. van der Ven, Montse Olivé, Hee-Suk Lee, Janbernd Kirschner, Piraye Serdaroglu-Oflazer, Dieter O. Fürst, Zagaa Odgerel, Rudolf A. Kley, Jörg Höhfeld, Matthias Vorgerd, Y. Hahn, Juan M. Bilbao
المصدر: Neuromuscular Disorders. 21:741
بيانات النشر: Elsevier BV, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Pathogenesis, Neurology, Pediatrics, Perinatology and Child Health, Myofibrillar myopathy, Neurology (clinical), Biology, Filamin, Phenotype, Genetics (clinical), Cell biology
تدمد: 0960-8966
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ff2bd45adecb5158e3e83c13bf0587e8Test
https://doi.org/10.1016/j.nmd.2011.06.1085Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........ff2bd45adecb5158e3e83c13bf0587e8
قاعدة البيانات: OpenAIRE