Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort.
cholesterol/metabolism
familial lecithin:cholesterol acyltransferase deficiency
high density lipoprotein
kidney transplantation
lecithin:cholesterol acyltransferase
lipoproteins
renal disease
Journal
Journal of lipid research
ISSN: 1539-7262
Titre abrégé: J Lipid Res
Pays: United States
ID NLM: 0376606
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
pubmed:
2
10
2020
medline:
26
10
2021
entrez:
1
10
2020
Statut:
ppublish
Résumé
Familial LCAT deficiency (FLD) is a rare genetic disorder of HDL metabolism, caused by loss-of-function mutations in the
Identifiants
pubmed: 32998975
pii: S0022-2275(20)60036-0
doi: 10.1194/jlr.P120000976
pmc: PMC7707181
pii:
doi:
Substances chimiques
Cholesterol
97C5T2UQ7J
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1784-1788Informations de copyright
Copyright © 2020 Pavanello et al.
Déclaration de conflit d'intérêts
Conflict of interest—Laura Calabresi has received research grants from MedImmune, Daiichi Sankyio, and Cerenis Therapeutics.
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