A carregar...

Mipomersen: evidence-based review of its potential in the treatment of homozygous and severe heterozygous familial hypercholesterolemia

Familial hypercholesterolemia (FH) is an autosomal-dominant inherited disease with a prevalence of one in 500 (heterozygous) to one in 1,000,000 (homozygous). Mutations of the low-density lipoprotein (LDL) receptor gene, the apolipoprotein B100 gene, or the PCSK9 gene may be responsible for the dise...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Autor principal: Parhofer, Klaus G
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3373191/
https://ncbi.nlm.nih.gov/pubmed/22701100
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CE.S25239
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!