[1]
E. ul H. Makhdoom, H. Anwar, S. M. Baig, and G. Hussain, “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, vol. 38, no. 1, Nov. 2021.