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[The mitochondrial genome and human mitochondrial diseases].
Sukernik RI, Derbeneva OA, Starikovskaia EB, Volod'ko NV, Mikhaĭlovskaia IE, Bychkov IIu, Lott M, Brown M, Wallace D. Sukernik RI, et al. Genetika. 2002 Feb;38(2):161-70. Genetika. 2002. PMID: 11898607 Review. Russian.
African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes.
Ke Y, Su B, Song X, Lu D, Chen L, Li H, Qi C, Marzuki S, Deka R, Underhill P, Xiao C, Shriver M, Lell J, Wallace D, Wells RS, Seielstad M, Oefner P, Zhu D, Jin J, Huang W, Chakraborty R, Chen Z, Jin L. Ke Y, et al. Science. 2001 May 11;292(5519):1151-3. doi: 10.1126/science.1060011. Science. 2001. PMID: 11349147
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy.
Bannwarth S, Procaccio V, Rouzier C, Fragaki K, Poole J, Chabrol B, Desnuelle C, Pouget J, Azulay JP, Attarian S, Pellissier JF, Gargus JJ, Abdenur JE, Mozaffar T, Calvas P, Labauge P, Pages M, Wallace DC, Lambert JC, Paquis-Flucklinger V. Bannwarth S, et al. Among authors: wallace dc. Mitochondrion. 2008 Mar;8(2):136-45. doi: 10.1016/j.mito.2007.10.008. Epub 2007 Nov 6. Mitochondrion. 2008. PMID: 18078792
513 results