Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Muthaffar, Osama Yousef, Sogaty, Sameera, Alkhatabi, Hiba, Almaghrabi, Sarah, Chaudhary, Adeel G.
Publicado 2021