ARSB mutants:Ca2+ [lysosomal lumen]

Stable Identifier
R-HSA-9631731
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Disease
Name Identifier Synonyms
mucopolysaccharidosis VI 12800 Maroteaux-Lamy syndrome, arylsulfatase B deficiency, Maroteaux - Lamy syndrome, Maroteaux-Lamy syndrome (disorder), deficiency of N-acetylgalactosamine-4-sulfatase (disorder)