Author:
Bashir Rumaisa,Britton Stephen,Strachan Tom,Keers Sharon,Vafiadaki Elizabeth,Lako Majlinda,Richard Isabelle,Marchand Sylvie,Bourg Nathalie,Argov Zohar,Sadeh Menachem,Mahjneh Ibrahim,Marconi Giampiero,Passos-Bueno Maria Rita,Moreira Eloisa de S,Zatz Mayana,Beckmann Jacques S.,Bushby Kate
Publisher
Springer Science and Business Media LLC
Reference48 articles.
1. Koenig, M. et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50, 509– 517 (1987).
2. Bushby, K.M.D. The limb-girdle muscular dystrophies. in Diagnostic Criteria for Neuromuscular Disorders (ed. Emery, A.E.H.) 17– 22 (Royal Society of Medicine Press, London, 1997).
3. Worton, R.G. Muscular dystrophies: diseases of the dystrophin-glycoprotein complex. Science 270, 755–756 ( 1995).
4. Noguchi, S. et al. Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy. Science 270, 819–822 (1995).
5. Piccolo, F. et al. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity. Nature Genet. 10, 243–245 (1995).
Cited by
584 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