1. Clinical and genetic variations in the syndrome of adult GM2 gangliodosis resulting from hexosaminidase a deficiency
2. Calnexin: a membrane-bound chaperone of the endoplasmic reticulum
3. Hexosaminidase isozyme in type O GM2 gangliosidosis (Sandhoff–Jatzkewitz disease);Beutler E;American Journal of Human Genetics,1975
4. Xmnl RFLP at 5q13 detected by a 0.49 kb Xmn I fragment of human hexosaminidase (HEXB) cDNA
5. β‐Hexosaminidase isozymes from cells co‐transfected with α and β cDNA constructs: analysis of α subunit missense mutation associated with the adult form of Tay–Sachs disease;Brown CA;American Journal of Human Genetics,1993