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Selected References
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- Moraes C. T., Shanske S., Tritschler H. J., Aprille J. R., Andreetta F., Bonilla E., Schon E. A., DiMauro S. mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases. Am J Hum Genet. 1991 Mar;48(3):492–501. [PMC free article] [PubMed] [Google Scholar]
- Seibel P., Degoul F., Romero N., Marsac C., Kadenbach B. Identification of point mutations by mispairing PCR as exemplified in MERRF disease. Biochem Biophys Res Commun. 1990 Dec 14;173(2):561–565. doi: 10.1016/s0006-291x(05)80071-3. [DOI] [PubMed] [Google Scholar]
- Tanaka M., Ino H., Ohno K., Hattori K., Sato W., Ozawa T., Tanaka T., Itoyama S. Mitochondrial mutation in fatal infantile cardiomyopathy. Lancet. 1990 Dec 8;336(8728):1452–1452. doi: 10.1016/0140-6736(90)93162-i. [DOI] [PubMed] [Google Scholar]
- Yoon K. L., Aprille J. R., Ernst S. G. Mitochondrial tRNA(thr) mutation in fatal infantile respiratory enzyme deficiency. Biochem Biophys Res Commun. 1991 May 15;176(3):1112–1115. doi: 10.1016/0006-291x(91)90399-r. [DOI] [PubMed] [Google Scholar]
- Zheng X., Shoffner J. M., Lott M. T., Voljavec A. S., Krawiecki N. S., Winn K., Wallace D. C. Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV. Neurology. 1989 Sep;39(9):1203–1209. doi: 10.1212/wnl.39.9.1203. [DOI] [PubMed] [Google Scholar]