Search Results - Aziz Mhanni

  • Showing 1 - 2 results of 2
Refine Results
  1. 1

    A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review by Aisha Al Shamsi, Noura Al Hassani, Moustafa Hamchou, Raya Almazrouei, Aziz Mhanni

    Published in Molecular Genetics & Genomic Medicine (2020-11-01)
    Get full text
    Article


  2. 2

    Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndrome by Tamar Rubin, Stéphane Bernier, Lily Siok Hoon Lim, Michael S. Salman, Edward Leung, Aziz Mhanni, Sandra Marles, Cheryl Greenberg, Anna Perez, Yichun Sun, Isabelle Angers, Donald C. Vinh, Donald C. Vinh, Donald C. Vinh, Donald C. Vinh, Lucie Roussel

    Published in Frontiers in Immunology (2025-02-01)
    Get full text
    Article


Search Tools: