%0 Journal Article
%T A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
%A Adeel G. Chaudhary
%A Adel M. Abuzenadah
%A Haifa Mansour Mansour
%A Mahmood Rasool
%A Mohammad H. Al-Qahtani
%A Muhammad Imran Naseer
%A Rukhaa Adeel Chaudhary
%A Sameera Sogaty
%J Archive of "Annals of Saudi Medicine".
%D 2017
%R 10.5144/0256-4947.2017.148
%X Primary microcephaly (MCPH) is a rare developmental defect characterized by impaired cognitive functions, retarded neurodevelopment and reduced brain size. It is genetically heterogeneous and more than 17 genes so far have been identified that are associated with this disease
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150548/