APRT dimer mutants [cytosol]

Stable Identifier
R-HSA-9734185
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Disease
Name Identifier Synonyms
adenine phosphoribosyltransferase deficiency DOID:0060350 APRT deficiency, 2,8-dihydroxyadenine urolithiasis
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