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  • Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.

    Published in:
    Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0254-5
    By:
    • Koch, Johannes;
    • Freisinger, Peter;
    • Feichtinger, René G.;
    • Zimmermann, Franz A.;
    • Rauscher, Christian;
    • Wagentristl, Hans P.;
    • Konstantopoulou, Vassiliki;
    • Seidl, Rainer;
    • Haack, Tobias B.;
    • Prokisch, Holger;
    • Ahting, Uwe;
    • Sperl, Wolfgang;
    • Mayr, Johannes A.;
    • Maier, Esther M.
    Publication type:
    Article

  • Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.

    Published in:
    2015
    By:
    • Koch, Johannes;
    • Freisinger, Peter;
    • Feichtinger, René G;
    • Zimmermann, Franz A;
    • Rauscher, Christian;
    • Wagentristl, Hans P;
    • Konstantopoulou, Vassiliki;
    • Seidl, Rainer;
    • Haack, Tobias B;
    • Prokisch, Holger;
    • Ahting, Uwe;
    • Sperl, Wolfgang;
    • Mayr, Johannes A;
    • Maier, Esther M
    Publication type:
    journal article