Naseer, Muhammad Imran, Angham Abdulrahman Abdulkareem, Mohammed Mohammed Jan, Adeel G. Chaudhary, and Mohammad H. Al-Qahtani. 2020. “Whole Exome Sequencing Reveals a Homozygous Nonsense Mutation in HEXA Gene Leading to Tay-Sachs Disease in Saudi Family”. Pakistan Journal of Medical Sciences 36 (6). https://doi.org/10.12669/pjms.36.6.2579.