Mitochondrial Encephalomyopathies
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-662-41088-2_22
Reference62 articles.
1. Majamaa, K., J.S. Moilanen, S. Uimonen, et al. 1998. Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Am. J. Hum. Genet. 63: 447–454.
2. Darin, N., A. Oldfors, A.-R. Moslem, et al. 2001. The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities. Ann. Neurol. 49: 377–383.
3. Chinnery, P.F., T.M. Wardell, R. Singh-Kler, et al. 2000. The epidemiology of pathogenic mitochondrial DNA mutations. Ann. Neurol. 48: 188–193.
4. Chinnery, P.F. & D.M. Turnbull. 2001. Epidemiology and treatment of mitochondrial disorders. Am. J. Med. Genet. 106: 94–101.
5. Schon, E.A., M. Hirano & S. DiMauro. 2002. Molecular genetic basis of the mitochondrial encephalomyopathies. In Mitochondrial Disorders in Neurology 2. A.H. V. Schapira & S. DiMauro, Eds.: 69–113. Butterworth-Heinemann. Boston.
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