A novel homozygous frameshift mutation likely causing nonsense-mediated mRNA decay in an Algerian kindred with CD19 complex deficiency
在阿尔及利亚一个患有 CD19 复合物缺陷的家族中,发现了一种新的纯合移码突变,该突变可能导致无义介导的 mRNA 降解。
期刊:Frontiers in Immunology
影响因子:5.9
doi:10.3389/fimmu.2025.1634146
Belaid, Brahim; Chan, Koon-Wing; Lamara Mahammed, Lydia; Leung, Daniel; Makhloufi, Sara; Bendaoud, Fadila; Sakhri, Hassiba; Berkani, Lilya Meriem; Allam, Ines; Merah, Fatma; Baaziz, Hadda; Lo, Bernice; Rosa Duque, Jaime Sou; Lau, Yu Lung; Djidjik, Reda