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Published in 2019 at "Journal of Lipid Research"
DOI: 10.1194/jlr.ra119000154
Abstract: β-glucosidases [GBA1 (glucocerebrosidase) and GBA2] are ubiquitous essential enzymes. Lysosomal GBA1 and cytosol-facing GBA2 degrade glucosylceramide (GlcCer); GBA1 deficiency causes Gaucher disease, a lysosomal storage disorder characterized by lysosomal accumulation of GlcCer, which is partly…
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Keywords:
gba1 gba2;
gba2;
deficiency;
metabolism ... See more keywords