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Familial apolipoprotein E deficiency.

A unique kindred with premature cardiovascular disease, tubo-eruptive xanthomas, and type III hyperlipoproteinemia (HLP) associated with familial apolipoprotein (apo) E deficiency was examined. Homozygotes (n = 4) had marked increases in cholesterol-rich very low density lipoproteins (VLDL) and inte...

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Dades bibliogràfiques
Publicat a:J Clin Invest
Autors principals: Schaefer, E J, Gregg, R E, Ghiselli, G, Forte, T M, Ordovas, J M, Zech, L A, Brewer, H B
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 1986
Matèries:
Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423806/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3771793/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112704
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