New Approaches in Detection and Treatment of Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder that clinically leads to increased low density lipoprotein-cholesterol (LDL-C) levels. As a consequence, FH patients are at high risk for cardiovascular disease (CVD). Mutations are found in genes coding for the LDLR, apoB,...

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Detalles Bibliográficos
Autores principales: Hartgers, Merel L., Ray, Kausik K., Hovingh, G. Kees
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Lipid Abnormalities and Cardiovascular Prevention (G De Backer, Section Editor)
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611021/
https://www.ncbi.nlm.nih.gov/pubmed/26482752
http://dx.doi.org/10.1007/s11886-015-0665-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611021/
https://www.ncbi.nlm.nih.gov/pubmed/26482752
http://dx.doi.org/10.1007/s11886-015-0665-x

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