Mutational Analysis of the Portuguese Cohort with Clinical Diagnosis of Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid metabolism (1:500). FH patients present high levels of plasma cholesterol since birth, and if untreated, develop premature coronary heart disease (pCHD). To fulfil the World Health Organization recommendation (1998 r...

ver descrição completa

Detalhes bibliográficos
Autor principal: Medeiros, A.M. (author)
Outros Autores: Alves, A.C. (author), Bourbon, Mafalda (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2016
Assuntos:
Doenças Cardio e Cérebro-vasculares
Familial Hypercholesterolemia
Portugal
Texto completo:http://hdl.handle.net/10400.18/3375
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/3375

Texto Completo

http://hdl.handle.net/10400.18/3375

Registros relacionados