lysosomal-storage-disorder Downloads
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α-Galactosidase (also known as α-GAL or α-GAL A) is an enzyme that catalyzes the hydrolysis of the terminal α-galactosyl moieties of oligosaccharides and polysaccharides. Defects in human α-GAL result in Fabry disease, a rare lysosomal storage disorder belonging to sphingolipidoses that results from a failure to catabolize α-D-galactosyl glycolipid moieties. ...