A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy
作者
Muhammad Imran Naseer,Mohammad Khalid Alwasiyah,Angham Abdulrahman Abdulkareem,Rayan Abdullah Bajammal,Carlos Trujillo,Muhammad Abu‐Elmagd,Mohammad Jafri,Adeel Chaudhary,Mohammad H. Al-Qahtani