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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene.
Horváth R, Scharfe C, Hoeltzenbein M, Do BH, Schröder C, Warzok R, Vogelgesang S, Lochmüller H, Müller-Höcker J, Gerbitz KD, Oefner PJ, Jaksch M. Horváth R, et al. Among authors: do bh. J Med Genet. 2002 Nov;39(11):812-6. doi: 10.1136/jmg.39.11.812. J Med Genet. 2002. PMID: 12414820 Free PMC article. No abstract available.
The role of selection in the evolution of human mitochondrial genomes.
Kivisild T, Shen P, Wall DP, Do B, Sung R, Davis K, Passarino G, Underhill PA, Scharfe C, Torroni A, Scozzari R, Modiano D, Coppa A, de Knijff P, Feldman M, Cavalli-Sforza LL, Oefner PJ. Kivisild T, et al. Genetics. 2006 Jan;172(1):373-87. doi: 10.1534/genetics.105.043901. Epub 2005 Sep 19. Genetics. 2006. PMID: 16172508 Free PMC article.
Conservation of the RB1 gene in human and primates.
Sivakumaran TA, Shen P, Wall DP, Do BH, Kucheria K, Oefner PJ. Sivakumaran TA, et al. Among authors: do bh. Hum Mutat. 2005 Apr;25(4):396-409. doi: 10.1002/humu.20154. Hum Mutat. 2005. PMID: 15776430
64 results