Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

Familial defective apolipoprotein (apo) B-100 is a genetic disease that leads to hypercholesterolemia and to an increased serum concentration of low density lipoproteins that bind defectively to the apoB,E(LDL) receptor. The disorder appears to result from a mutation in the gene for apoB-100. Extens...

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Bibliografiska uppgifter
Huvudupphovsmän: Soria, L F, Ludwig, E H, Clarke, H R, Vega, G L, Grundy, S M, McCarthy, B J
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1989
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC286517/
https://ncbi.nlm.nih.gov/pubmed/2563166
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