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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

260 related items for PubMed ID: 17152068

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  • 17. Rapid identification of a novel complex I MT-ND3 m.10134C>A mutation in a Leigh syndrome patient.
    Miller DK, Menezes MJ, Simons C, Riley LG, Cooper ST, Grimmond SM, Thorburn DR, Christodoulou J, Taft RJ.
    PLoS One; 2014; 9(8):e104879. PubMed ID: 25118196
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  • 18. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
    Leng Y, Liu Y, Fang X, Li Y, Yu L, Yuan Y, Wang Z.
    Mitochondrial DNA; 2015 Apr; 26(2):208-12. PubMed ID: 24708134
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  • 19. Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome.
    Ugalde C, Hinttala R, Timal S, Smeets R, Rodenburg RJ, Uusimaa J, van Heuvel LP, Nijtmans LG, Majamaa K, Smeitink JA.
    Mol Genet Metab; 2007 Jan; 90(1):10-4. PubMed ID: 16996290
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