Naseer MI, Rasool M, Abdulkareem AA, Chaudhary AG, Zaidi SK, Al-Qahtani MH. Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family: A novel compound heterozygous mutation in WDR62gen. Pak J Med Sci [Internet]. 2019May21 [cited 2024Apr.27];35(3). Available from: https://pjms.org.pk/index.php/pjms/article/view/36