1.
Naseer MI, Abdulkareem AA, Jan MM, Chaudhary AG, Al-Qahtani MH. Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family. Pak J Med Sci [Internet]. 2020Aug.20 [cited 2024Mar.29];36(6). Available from: https://pjms.org.pk/index.php/pjms/article/view/2579