Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome).
Alfadhel M, Alhubayshi BS, Umair M, Alfaidi A, Alwadaani D, Aloyouni E, Abbas S, Abdulrahman AA, Aldrees M, Tuwaijri AA, Alharithy RS, Alajlan A, Alswaid A, Almohrij S, Al-Khenaizan S.
Alfadhel M, et al. Among authors: abbas s.
Genet Mol Biol. 2025 Jan 20;48(1):e20240094. doi: 10.1590/1678-4685-GMB-2024-0094. eCollection 2025.
Genet Mol Biol. 2025.
PMID: 39846792