Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference11 articles.
1. Hereditary neuromuscular disorders in children;Goebel;Semin Pediatr Neurol,2002
2. Neuromuscular disorders: Gene location (gene table);Kaplan;Neuromuscul Disord,2006
3. Mutations in dynamin 2 cause dominant centronuclear myopathy;Bitoun;Nat Genet,2005
4. Autosomal dominant mutations in the human ryanodine receptor (RYR1) gene associated with centronuclear myopathy;Jungbluth;Neuromuscul Disord,2005
5. Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H;Schoser;Ann Neurol,2005
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献