Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity M. Dehmel,H. Hu,T. F. Wienker,L. Musante, H. H. Ropers,Angela Huebner,A Kaindl,M. von der HagenNeuropediatrics（2016）引用 1|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
