Works matching IS 09462716 AND DT 2002 AND VI 80 AND IP 2


Results: 8
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    Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients.

    Published in:
    Journal of Molecular Medicine, 2002, v. 80, n. 2, p. 124, doi. 10.1007/s00109-001-0310-6
    By:
    • Wattenhofer, Marie;
    • Di Iorio, Mario;
    • Rabionet, Raquel;
    • Dougherty, Loretta;
    • Pampanos, Andreas;
    • Schwede, Torsten;
    • Montserrat-Sentis, Barbara;
    • Arbones, Maria;
    • Iliades, Theofilos;
    • Pasquadibisceglie, Annamaria;
    • D'Amelio, Marcello;
    • Alwan, Sura;
    • Rossier, Colette;
    • Dahl, Hans-Henrik M.;
    • Petersen, Michael B.;
    • Estivill, Xavier;
    • Gasparini, Paolo;
    • Scott, Hamish S.;
    • Antonarakis, Stylianos E.
    Publication type:
    Article