Diagnostic Challenges of Mitochondrial Disorders: Complexities of Two Genomes
Reference38 articles.
1. Haas, R. H., Parikh, S., Falk, M. J., Saneto, R. P., Wolf, N. I., Darin, N., and Cohen, B. H. (2007) Mitochondrial disease: a practical approach for primary care physicians, Pediatrics 120, 1326–1333. 2. Haas, R. H., Parikh, S., Falk, M. J., Saneto, R. P., Wolf, N. I., Darin, N., Wong, L. J., Cohen, B. H., and Naviaux, R. K. (2008) The in-depth evaluation of suspected mitochondrial disease, Mol Genet Metab 94, 16–37. 3. Bernier, F. P., Boneh, A., Dennett, X., Chow, C. W., Cleary, M. A., and Thorburn, D. R. (2002) Diagnostic criteria for respiratory chain disorders in adults and children, Neurology 59, 1406–1411. 4. Wolf, N. I., and Smeitink, J. A. (2002) Mitochondrial disorders: a proposal for consensus diagnostic criteria in infants and children, Neurology 59, 1402–1405. 5. Skladal, D., Halliday, J., and Thorburn, D. R. (2003) Minimum birth prevalence of mitochondrial respiratory chain disorders in children, Brain 126, 1905–1912.
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