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- Goto Y., Nonaka I., Horai S. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature. 1990 Dec 13;348(6302):651–653. doi: 10.1038/348651a0. [DOI] [PubMed] [Google Scholar]
- Howell N., McCullough D. An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene. Am J Hum Genet. 1990 Oct;47(4):629–634. [PMC free article] [PubMed] [Google Scholar]
- Huoponen K., Vilkki J., Savontaus M. L., Aula P., Nikoskelainen E. K. Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy. Genomics. 1990 Nov;8(3):583–585. doi: 10.1016/0888-7543(90)90049-z. [DOI] [PubMed] [Google Scholar]
- Lertrit P., Noer A. S., Jean-Francois M. J., Kapsa R., Dennett X., Thyagarajan D., Lethlean K., Byrne E., Marzuki S. A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I. Am J Hum Genet. 1992 Sep;51(3):457–468. [PMC free article] [PubMed] [Google Scholar]
- Ozawa T., Tanaka M., Sugiyama S., Ino H., Ohno K., Hattori K., Ohbayashi T., Ito T., Deguchi H., Kawamura K. Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy. Biochem Biophys Res Commun. 1991 May 31;177(1):518–525. doi: 10.1016/0006-291x(91)92014-b. [DOI] [PubMed] [Google Scholar]
- Sakuta R., Goto Y., Horai S., Nonaka I. Mitochondrial DNA mutations at nucleotide positions 3243 and 3271 in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes: a comparative study. J Neurol Sci. 1993 Apr;115(2):158–160. doi: 10.1016/0022-510x(93)90219-o. [DOI] [PubMed] [Google Scholar]
- Shoffner J. M., Lott M. T., Lezza A. M., Seibel P., Ballinger S. W., Wallace D. C. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell. 1990 Jun 15;61(6):931–937. doi: 10.1016/0092-8674(90)90059-n. [DOI] [PubMed] [Google Scholar]
- Wallace D. C., Singh G., Lott M. T., Hodge J. A., Schurr T. G., Lezza A. M., Elsas L. J., 2nd, Nikoskelainen E. K. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science. 1988 Dec 9;242(4884):1427–1430. doi: 10.1126/science.3201231. [DOI] [PubMed] [Google Scholar]