Evaluation of the role of STAP1 in Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is characterised by elevated serum levels of low-density lipoprotein cholesterol (LDL-C) and a substantial risk for cardiovascular disease. The autosomal-dominant FH is mostly caused by mutations in LDLR (low density lipoprotein receptor), APOB (apolipoprotein B),...

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Publicat a:Sci Rep
Autors principals: Danyel, Magdalena, Ott, Claus-Eric, Grenkowitz, Thomas, Salewsky, Bastian, Hicks, Andrew A., Fuchsberger, Christian, Steinhagen-Thiessen, Elisabeth, Bobbert, Thomas, Kassner, Ursula, Demuth, Ilja
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2019
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6700100/
https://ncbi.nlm.nih.gov/pubmed/31427613
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-48402-y
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