Myofibrillar myopathy associated with filamin C mutations: Refining the phenotype and new insights in pathogenesisM. Vorgerd, R. A. Kley, P. Serdaroglu-Oflazer,Z. Odgerel,M. Olive,H. S. Lee,Y. Hahn,P. F. M. van der Ven,J. Hoehfeld,J. Kirschner, J. M. Bilbao, L. G. Goldfarb, D. O. FuerstNeuromuscular Disorders(2011)引用 0|浏览22暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要