Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cows.

Patients with familial dysbetalipoproteinemia (F. Dys.), also called familial type 3 hyperlipoproteinemia, are homozygous for a mutant allele, Ed, that specifies an abnormal form of apoprotein (apo) E, a prominent constituent of remnant lipoproteins derived from very low density lipoproteins (VLDL)...

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Dades bibliogràfiques
Publicat a:	J Clin Invest
Autors principals:	Schneider, W J, Kovanen, P T, Brown, M S, Goldstein, J L, Utermann, G, Weber, W, Havel, R J, Kotite, L, Kane, J P, Innerarity, T L, Mahley, R W
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Clinical Investigation 1981
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370895/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6270194/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110330
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Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cows.

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