Diseases of the Human Mitochondrial Oxidative Phosphorylation System-Reference-Cited by-同舟云学术

Diseases of the Human Mitochondrial Oxidative Phosphorylation System

Published:2009 Issue: Volume: Page:47-67
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
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Author:

Montoya Julio,López-Gallardo Ester,Herrero-Martín María Dolores,Martínez-Romero Íñigo,Gómez-Durán Aurora,Pacheu David,Carreras Magdalena,Díez-Sánchez Carmen,López-Pérez Manuel J.,Ruiz-Pesini Eduardo

Publisher

Springer Netherlands

Link

http://link.springer.com/content/pdf/10.1007/978-90-481-2813-6_5.pdf

Reference61 articles.

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4. Bindoff, L. A., Howell, N., Poulton, J., Mccullough, D. A., Morten, K. J., Lightowlers, R. N., Turnbull, D. M. and Weber, K. Abnormal RNA processing associated with a novel transfer RNA mutation in mitochondrial DNA - a potential disease mechanism. J Biol Chem (1993) 268: 19559–19564.

5. Bourgerom, T., Rustin, P., Chretien, D., Birch-Machin, M., Bourgeois, M., Viegas-Pequignot, E., Munnich, A. and Rotig, A. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nat Genet (1995) 11: 144–149.

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