Naseer, M. I., Abdulkareem, A. A., Jan, M. M., Chaudhary, A. G., & Al-Qahtani, M. H. (2020). Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family. Pak J Med Sci.

Naseer, Muhammad Imran, Angham Abdulrahman Abdulkareem, Mohammed Mohammed Jan, Adeel G. Chaudhary, ja Mohammad H. Al-Qahtani. "Whole Exome Sequencing Reveals a Homozygous Nonsense Mutation in HEXA Gene Leading to Tay-Sachs Disease in Saudi Family." Pak J Med Sci 2020.

Naseer, Muhammad Imran, et al. "Whole Exome Sequencing Reveals a Homozygous Nonsense Mutation in HEXA Gene Leading to Tay-Sachs Disease in Saudi Family." Pak J Med Sci 2020.