A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities.

Epidemiologic data of recent years have identified an important role of HDL deficiency in the etiology of atherosclerosis. Biochemical data suggest that some of these deficiencies may be a consequence of defects in the structural genes of HDL apolipoproteins or of plasma enzymes that modify HDL. We...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:J Clin Invest
Main Authors: Funke, H, von Eckardstein, A, Pritchard, P H, Karas, M, Albers, J J, Assmann, G
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1991
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295069/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1898657/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114997
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker