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)...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Jones, Christopher, Garuti, Rita, Michaely, Peter, Li, Wei-Ping, Maeda, Nobuyo, Cohen, Jonathan C., Herz, Joachim, Hobbs, Helen H.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2007
Assuntos:
Research Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados