Abnormal LAMP1 glycosylation may play a role in Niemann-Pick disease, type C pathology
Niamh X. Cawley(National Institutes of Health), Forbes D. Porter(National Institutes of Health)
Cited by 35
Related Papers
Characterization of placental cholesterol transport: ABCA1 is a potential target for in utero therapy of Smith-Lemli-Opitz syndrome
|Human Molecular Genetics|2008|72
Necroptosis in Niemann–Pick disease, type C1: a potential therapeutic target
|Cell Death and Disease|2016|56