Works matching AU Ogier, Heléne

Results: 1
    1

    New spastic paraplegia phenotype associated to mutation of NFU1.

    Published in:
    Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0237-6
    By:
    • Tonduti, Davide;
    • Dorboz, Imen;
    • Imbard, Apolline;
    • Slama, Abdelhamid;
    • Boutron, Audrey;
    • Pichard, Samia;
    • Elmaleh, Monique;
    • Vallée, Louis;
    • Benoist, Jean François;
    • Ogier, Heléne;
    • Boespflug-Tanguy, Odile
    Publication type:
    Article