Sign Up to like & get
recommendations!
1
Published in 2022 at "Journal of lipid research"
DOI: 10.1016/j.jlr.2022.100199
Abstract: In Gaucher disease (GD), the deficiency of glucocerebrosidase (GCase/ GBA1) causes lysosomal accumulation of glucosylceramide (GlcCer), which is partly converted by acid ceramidase (ACase) to glucosylsphingosine (GlcSph) in the lysosome. Chronically elevated blood and tissue…
read more here.
Keywords:
glcsph;
deficient zebrafish;
glucocerebrosidase deficient;
excessive glcsph ... See more keywords