Interconversion of Human Lysosomal Enzyme Specificities Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, Alpha-galactosidase A, GLYCEROL, ... Authors: Tomasic, I.B, Metcalf, M.C, Guce, A.I, Clark
Tay-Sachs disease (TSD) is a inherited lysosomal storage disease resulting from mutations in the α-subunits of the lysosomal enzyme, β-hexosaminidase A, and leads to excessive accumulation of GM2 gang
