1.
Makhdoom E ul H, Anwar H, Baig SM, Hussain G. Whole exome sequencing identifies a novel mutation in ASPM and ultra-rare mutation in CDK5RAP2 causing Primary microcephaly in consanguineous Pakistani families. Pak J Med Sci [Internet]. 2021Nov.22 [cited 2024Apr.19];38(1). Available from: https://pjms.org.pk/index.php/pjms/article/view/4464