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.
Autor principal: | |
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Formato: | lecture |
Idioma: | eng |
Publicado em: |
2019
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Assuntos: | |
Texto completo: | http://hdl.handle.net/10400.18/5877 |
País: | Portugal |
Oai: | oai:repositorio.insa.pt:10400.18/5877 |