Author:
Boyden Steven E.,Mahoney Lane J.,Kawahara Genri,Myers Jennifer A.,Mitsuhashi Satomi,Estrella Elicia A.,Duncan Anna R.,Dey Friederike,DeChene Elizabeth T.,Blasko-Goehringer Jessica M.,Bönnemann Carsten G.,Darras Basil T.,Mendell Jerry R.,Lidov Hart G. W.,Nishino Ichizo,Beggs Alan H.,Kunkel Louis M.,Kang Peter B.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics (clinical),Genetics
Reference48 articles.
1. Kaplan JC (2010) The 2011 version of the gene table of neuromuscular disorders. Neuromuscul Disord 20:852–873
2. Sewry CA (2008) Pathological defects in congenital myopathies. J Muscle Res Cell Motil 29:231–238
3. Dalkilic I, Kunkel LM (2003) Muscular dystrophies: genes to pathogenesis. Curr Opin Genet Dev 13:231–238
4. Engel AG, Gomez MR, Groover RV (1971) Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers. Mayo Clin Proc 46:666–681
5. Moghadaszadeh B, Petit N, Jaillard C, Brockington M, Roy SQ, Merlini L, Romero N, Estournet B, Desguerre I, Chaigne D, Muntoni F, Topaloglu H, Guicheney P (2001) Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome. Nat Genet 29:17–18
Cited by
65 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