Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.

Familial defective apolipoprotein (apo) B-100 is a recently described genetic disorder that appears to result from a mutation in the apoB-100 gene. This disorder is characterized by hypercholesterolemia resulting from elevated plasma concentrations of low density lipoprotein LDL. The disorder was fi...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Weisgraber, K H, Innerarity, T L, Newhouse, Y M, Young, S G, Arnold, K S, Krauss, R M, Vega, G L, Grundy, S M, Mahley, R W
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1988
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC282860/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3200853/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.24.9758
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