Pharmacogenetic aspects in familial hypercholesterolemia with the special focus on FH(Marburg) (FH p.W556R)

OBJECTIVE: Familial hypercholesterolemia (FH) is an autosomal dominant inherited disorder caused by mutations in the low density lipoprotein receptor (LDLR) gene. FH is characterized by elevated plasma LDL cholesterol, premature atherosclerosis, and a high risk of premature myocardial infarction. In...

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Detalles Bibliográficos
Autores principales: Schaefer, Juergen R., Kurt, Bilgen, Sattler, Alexander, Klaus, Günter, Soufi, Muhidien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374117/
https://www.ncbi.nlm.nih.gov/pubmed/22528129
http://dx.doi.org/10.1007/s11789-012-0041-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374117/
https://www.ncbi.nlm.nih.gov/pubmed/22528129
http://dx.doi.org/10.1007/s11789-012-0041-y

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