Author:
Ruitenbeek W.,Wendel U.,Hamel B. C. J.,Trijbels J. M. F.
Subject
Genetics(clinical),Genetics
Reference33 articles.
1. Adams, PL, Turnbull D (1996) Disorders of the electron transport chain.J Inher Metab Dis 19: 463–469.
2. Barth PG, Scholte HR, Berden JA, et al (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.J Neurol Sci 62: 327–355.
3. Bolhuis PA, Hensels GW, Hulsebos TJM, Baas F, Barth PG (1991) Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.Am J Hum Genet 48: 481–485.
4. Bourgeron T, Chretien D, Poggi-Bach J, et al (1994) Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.J Clin Invest 93: 2514–2518.
5. Bourgeron T, Rustin P, Chretien D, et al (1995) Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.Nature Genetics 11: 144–149.
Cited by
24 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