Works matching IS 08830738 AND DT 2017 AND VI 32 AND IP 8


Results: 13
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13

    Clinical, Molecular, and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-hook1 Cluster in Rett Syndrome.

    Published in:
    Journal of Child Neurology, 2017, v. 32, n. 8, p. 694, doi. 10.1177/0883073817701622
    By:
    • Kharrat, Marwa;
    • Kamoun, Yosra;
    • Kamoun, Fatma;
    • Ellouze, Emna;
    • Maalej, Marwa;
    • Fendri-Kriaa, Nourhene;
    • Ammar-Keskes, Leila;
    • Belghith, Neila;
    • Gargouri, Ali;
    • Triki, Chahnez;
    • Fakhfakh, Faiza
    Publication type:
    Article