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Clinical implications of duplicated mtDNA in Pearson syndrome.
Muraki K, Sakura N, Ueda H, Kihara H, Goto Y. Muraki K, et al. Among authors: goto y. Am J Med Genet. 2001 Jan 22;98(3):205-9. doi: 10.1002/1096-8628(20010122)98:3<205::aid-ajmg1077>;2-p. Am J Med Genet. 2001. PMID: 11169556
Adult Leigh syndrome with mitochondrial DNA mutation at 8993.
Nagashima T, Mori M, Katayama K, Nunomura M, Nishihara H, Hiraga H, Tanaka S, Goto Y, Nagashima K. Nagashima T, et al. Among authors: goto y. Acta Neuropathol. 1999 Apr;97(4):416-22. doi: 10.1007/s004010051007. Acta Neuropathol. 1999. PMID: 10208283 Review.
4,198 results