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Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease.
EBioMedicine. 2023 Jun;92:104628. doi: 10.1016/j.ebiom.2023.104628. Epub 2023 May 26.
EBioMedicine. 2023.
PMID: 37245481
Free PMC article.
Lysosomal phospholipase A2 contributes to the biosynthesis of the atypical late endosome lipid bis(monoacylglycero)phosphate.
Chen J, Cazenave-Gassiot A, Xu Y, Piroli P, Hwang R Jr, DeFreitas L, Chan RB, Di Paolo G, Nandakumar R, Wenk MR, Marquer C.
Chen J, et al. Among authors: hwang r jr.
Commun Biol. 2023 Feb 23;6(1):210. doi: 10.1038/s42003-023-04573-z.
Commun Biol. 2023.
PMID: 36823305
Free PMC article.
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