Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Reference83 articles.
1. Engel AG, Gomez MR, Groover RV: Multicore disease. Mayo Clin Proc. 1971, 10: 666-681.
2. Wallgren-Pettersson C: Congenital nemaline myopathy: a longitudinal study. 1990, Academic dissertation, University of Helsinki, Commentationes Physico-Mathematicae 111/Dissertationes, 30: 102-
3. Hughes MI, Hicks EM, Nevin NC, Patterson VH: The prevalence of inherited neuromuscular disease in Northern Ireland. Neuromuscul Disord. 1996, 6: 69-73. 10.1016/0960-8966(94)00017-4.
4. Darin N, Tulinius M: Neuromuscular disorders in childhood: a descriptive epidemiological study from Western Sweden. Neuromuscul Disord. 2000, 10: 1-9. 10.1016/S0960-8966(99)00055-3.
5. Zhang Y, Chen HS, Khanna VK, DeLeon S, Phillips MS, Schappert K, Britt BA, Browell AK, MacLennan DH: A mutation in the human ryanodine receptor associated with central core disease. Nature Genetics. 1993, 5: 46-50. 10.1038/ng0993-46.
Cited by
109 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