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