Works by Al‐Balool, Haya H.

Results: 3
    1
    2

    Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3′‐end processing.

    Published in:
    Human Mutation, 2019, v. 40, n. 10, p. 1731, doi. 10.1002/humu.23777
    By:
    • Saoura, Makenzie;
    • Powell, Christopher A.;
    • Kopajtich, Robert;
    • Alahmad, Ahmad;
    • AL‐Balool, Haya H.;
    • Albash, Buthaina;
    • Alfadhel, Majid;
    • Alston, Charlotte L.;
    • Bertini, Enrico;
    • Bonnen, Penelope E.;
    • Bratkovic, Drago;
    • Carrozzo, Rosalba;
    • Donati, Maria A.;
    • Di Nottia, Michela;
    • Ghezzi, Daniele;
    • Goldstein, Amy;
    • Haan, Eric;
    • Horvath, Rita;
    • Hughes, Joanne;
    • Invernizzi, Federica
    Publication type:
    Article
    3

    Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis.

    Published in:
    Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2256
    By:
    • Alabdulrazzaq, Fatima;
    • Alanzi, Talal;
    • Al‐Balool, Haya H.;
    • Gardham, Alice;
    • Wakeling, Emma;
    • Leitch, Harry G.;
    • AlSayed, Moeenaldeen;
    • Abdulrahim, Maha;
    • Aladwani, Abdulaziz;
    • Romito, Antonio;
    • Kampe, Kapil;
    • Ferdinandusse, Sacha;
    • Aboelanine, Ashraf H.;
    • Abdullah, Amira;
    • Alwadani, Amal;
    • Bastaki, Laila;
    • Vaz, Frédéric M.;
    • Bertoli‐Avella, Aida M.;
    • Marafi, Dana
    Publication type:
    Article