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  • Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans.

    Published in:
    Human Genetics, 2020, v. 139, n. 4, p. 513, doi. 10.1007/s00439-020-02117-7
    By:
    • Seidahmed, Mohammed Zain;
    • Al-Kindi, Adila;
    • Alsaif, Hessa S.;
    • Miqdad, Abeer;
    • Alabbad, Nasser;
    • Alfifi, Abdallah;
    • Abdelbasit, Omer Bashir;
    • Alhussein, Khalid;
    • Alsamadi, Abdulmohsen;
    • Ibrahim, Niema;
    • Al-Futaisi, Amna;
    • Al-Maawali, Almundher;
    • Alkuraya, Fowzan S.
    Publication type:
    Article