Found: 2

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  • A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

    Published in:
    Nature Genetics, 2001, v. 28, n. 3, p. 213, doi. 10.1038/90038
    By:
    • Njajou, Omer T.;
    • Vaessen, Norbert;
    • Joosse, Marijke;
    • Berghuis, Bianca;
    • van Dongen, Jeroen W.F.;
    • Breuning, Martijn H.;
    • Snijders, Pieter J.L.M.;
    • Rutten, Wim P.F.;
    • Sandkuijl, Lodewijk A.;
    • Oostra, Ben A.;
    • van Duijn, Cornelia M.;
    • Heutink, Peter
    Publication type:
    Article

  • Mutations in TITF-1 are associated with benign hereditary chorea.

    Published in:
    Human Molecular Genetics, 2002, v. 11, n. 8, p. 971, doi. 10.1093/hmg/11.8.971
    By:
    • Breedveld, Guido J.;
    • van Dongen, Jeroen W.F.;
    • Danesino, Cesare;
    • Guala, Andrea;
    • Percy, Alan K.;
    • Dure, Leon S.;
    • Harper, Peter;
    • Lazarou, Lazarus P.;
    • van der Linde, Herma;
    • Joosse, Marijke;
    • Grüters, Annette;
    • MacDonald, Marcy E.;
    • de Vries, Bert B.A.;
    • Arts, Willem Frans M.;
    • Oostra, Ben A.;
    • Krude, Heiko;
    • Heutink, Peter
    Publication type:
    Article