Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemia

Genetic defects in LDL clearance result in severe hypercholesterolemia and premature atherosclerosis. Mutations in the LDL receptor (LDLR) cause familial hypercholesterolemia (FH), the most severe form of genetic hypercholesterolemia. A phenocopy of FH, autosomal recessive hypercholesterolemia (ARH)...

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Detaylı Bibliyografya
Asıl Yazarlar: Jones, Christopher, Garuti, Rita, Michaely, Peter, Li, Wei-Ping, Maeda, Nobuyo, Cohen, Jonathan C., Herz, Joachim, Hobbs, Helen H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Clinical Investigation 2007
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716209/
https://ncbi.nlm.nih.gov/pubmed/17200716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI29415
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