Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799168
Reference16 articles.
1. Arts WF, Scholte HR, Loonen MC, et al (1987) Cytochromec oxidase deficiency in subacute necrotizing encephalomyelopathy.J Neurol Sci 77: 103–115.
2. DiMauro S, Servidei S, Zeviani M, et al (1987) Cytochromec oxidase deficiency in Leigh syndrome.Ann Neurol 22: 498–506.
3. Di-Rocco M, Veneselli E, Ciccone MO, Taccone A, Stroppiano M, Cottafava F (1988) Cytochromec oxidase deficiency in three patients with Leigh's disease.J Inher Metab Dis 11: 189–192.
4. Glerum DM, Yanamura W, Capaldi RA, Robinson BH (1988) Characterization of cytochrome-c oxidase mutants in human fibroblasts.FEBS Lett 236: 100–104.
5. Hayasaka K, Brown GK, Danks DM, Droste M, Kadenbach B (1989) Cytochromec oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).J Inher Metab Dis 12: 247–256.
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