Found: 2

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  • High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 851, doi. 10.1038/ng.659
    By:
    • Calvo, Sarah E.;
    • Tucker, Elena J.;
    • Compton, Alison G.;
    • Kirby, Denise M.;
    • Crawford, Gabriel;
    • Burtt, Noel P.;
    • Rivas, Manuel;
    • Guiducci, Candace;
    • Bruno, Damien L.;
    • Goldberger, Olga A.;
    • Redman, Michelle C.;
    • Wiltshire, Esko;
    • Wilson, Callum J.;
    • Altshuler, David;
    • Gabriel, Stacey B.;
    • Daly, Mark J.;
    • Thorburn, David R.;
    • Mootha, Vamsi K.
    Publication type:
    Article

  • Common variants at 30 loci contribute to polygenic dyslipidemia.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 56, doi. 10.1038/ng.291
    By:
    • Kathiresan, Sekar;
    • Willer, Cristen J.;
    • Peloso, Gina M;
    • Demissie, Serkalem;
    • Musunuru, Kiran;
    • Schadt, Eric E.;
    • Kaplan, Lee;
    • Bennett, Derrick;
    • Li, Yun;
    • Tanaka, Toshiko;
    • Voight, Benjamin F.;
    • Bonnycastle, Lori L.;
    • Jackson, Anne U.;
    • Crawford, Gabriel;
    • Surti, Aarti;
    • Guiducci, Candace;
    • Burtt, Noel P.;
    • Parish, Sarah;
    • Clarke, Robert;
    • Zelenika, Diana
    Publication type:
    Article