𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Plasma levels of PCSK9 and phenotypic variability in familial hypercholesterolemia

✍ Scribed by Michael, T.


Book ID
121389735
Publisher
Royal Society of Medicine Press
Year
2012
Tongue
English
Weight
73 KB
Volume
49
Category
Article
ISSN
0004-5632

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Novel mutations of the PCSK9 gene cause
✍ Delphine Allard; Sabine Amsellem; Marianne Abifadel; MΓ©lanie Trillard; Martine D πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 254 KB

Autosomal dominant hypercholesterolemia (ADH) is a frequent (1/500) monogenic inherited disorder characterized by isolated elevation of LDL leading to premature cardiovascular disease. ADH is known to result from mutations at two main loci: LDLR (encoding the low density lipoprotein receptor), and A