Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome)
截短的 SPAG9 作为一种新综合征的新候选基因:粗糙面部特征、白化病、白内障和发育迟缓(CACD 综合征)
期刊:Genetics and Molecular Biology
影响因子:1.7
doi:10.1590/1678-4685-GMB-2024-0094
Majid Alfadhel, Bashayr S Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Essra Aloyouni, Safdar Abbas, Abdulkareem Al Abdulrahman, Mohammed Aldrees, Abeer Al Tuwaijri, Ruaa S Alharithy, Abdulaziz Alajlan, Abdulrahman Alswaid, Saad Almohrij, Sultan Al-Khenaizan