Author:
Vazquez-Memije M. E.,Shanske S.,Santorelli F. M.,Kranz-Eble P.,Davidson E.,De Vivo D. C.,DiMauro S.
Subject
Genetics(clinical),Genetics
Reference21 articles.
1. Anderson S, Bankier, AT, Barrell BG, et al (1981) Sequence and organization of the human mitochondrial genome.Nature 290: 457–465.
2. Arts FWM, Scholte HR, Loonen MCB (1987) Cytochromec oxidase deficiency in subacute necrotizing encephalopathy.J Neurol Sci 77: 103–115.
3. Davis PC, Hoffman JC, Braun IF, Anmann P, Krawiecki N (1987) MR of Leigh's disease (subacute necrotizing encephalopathy).Am J Neurol Res 8: 71–75.
4. DiMauro S, Servidei S, Zeviani M, et al (1987) Cytochromec oxidase deficiency in Leigh syndrome.Ann Neurol 22: 498–506.
5. Holt IJ, Harding AE, Petty RKH, Morgan-Hughes JA (1990) A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.Am J Hum Genet 46: 428–433.
Cited by
56 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