Works by Walker, Winsome

Results: 2
    1

    Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

    Published in:
    Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513
    By:
    • Papadopoulou, Lefkothea C.;
    • Sue, Carolyn M.;
    • Davidson, Mercy M.;
    • Tanji, Kurenai;
    • Nishino, Ichizo;
    • Sadlock, James E.;
    • Krishna, Sindu;
    • Walker, Winsome;
    • Selby, Jeanette;
    • Glerum, D. Moira;
    • Coster, Rudy Van;
    • Lyon, Gilles;
    • Scalais, Emmanuel;
    • Lebel, Roger;
    • Kaplan, Paige;
    • Shanske, Sara;
    • De Vivo, Darryl C.;
    • Bonilla, Eduardo;
    • Hirano, Michio
    Publication type:
    Article
    2

    A functionally dominant mitochondrial DNA mutation.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 12, p. 1814, doi. 10.1093/hmg/ddn073
    By:
    • Sacconi, Sabrina;
    • Salviati, Leonardo;
    • Nishigaki, Yutaka;
    • Walker, Winsome F.;
    • Hernandez-Rosa, Evelyn;
    • Trevisson, Eva;
    • Delplace, Severine;
    • Desnuelle, Claude;
    • Shanske, Sara;
    • Hirano, Michio;
    • Schon, Eric A.;
    • Bonilla, Eduardo;
    • De Vivo, Darryl C.;
    • DiMauro, Salvatore;
    • Davidson, Mercy M.
    Publication type:
    Article