1. Kristensson K, Sourander P, Svennerholm L. Tay-Sachs disease: A generalised metabolic disorder.Acta Paediatr Scand 1966; 55 :546–562.
2. Volk BW, Adachi M, Scheck L, Klienberg W. G5-ganglioside variant of systemic late infantile lipidosis.Arch Pathol 1969; 87:393–403.
3. Volk W, Schneck L, Adachi. Clinic, pathology and biochemistry of Tay-Sachs disease. In Vinkyn PJ and Bruyn GW, eds.Handbook of Clinical Neurology. Amsterdam, North-Holland Publishing company, 1970; 385–426.
4. Kumta NB, Irani SF, Bhide AR, Punwami DV. Hexosaminidase A deficiency (Tay-Sachs disease) : A rare inborn error of ganglioside metabolism in India. In Verma IC, ed.Medical Genetics in India. Pondicherry Auroma Enterprises, 1978; 1: 97–102.
5. Multicentric study on Genetic Counselling and Antenatal Diagnosis by ICMR Task Force on Human Genetics. 1984–87.