[1]
M. I. Naseer, A. A. Abdulkareem, M. M. Jan, A. G. Chaudhary, and M. 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, vol. 36, no. 6, Aug. 2020.