Estudo português de Hipercolesterolaemia Familiar

Main Aim: To identify the cause of the dyslipidaemia in patients with a clinical phenotype of Familial Hypercholesterolaemia (FH). Secondary aims: To implement the genetic diagnosis of FH; To perform an epidemiological study of FH; To study the pathophysiology of premature CHD in FH patients.

Detalhes bibliográficos
Autor principal: Bourbon, Mafalda (author)
Formato: lecture
Idioma:eng
Publicado em: 2019
Assuntos:
Texto completo:http://hdl.handle.net/10400.18/5877
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/5877