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Genetic screening for homozygous and heterozygous familial hypercholesterolemia

Familial hypercholesterolemia (FH) is a common inherited disorder that results in premature atherosclerosis. Diagnosis of FH is suspected on the basis of clinical criteria, but confirmation requires genetic testing. In the era of statins, early diagnosis and initiation of treatment can modify diseas...

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Detalhes bibliográficos
Main Authors: Izar, Maria C, Machado, Valéria A, Fonseca, Francisco A
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3681171/
https://ncbi.nlm.nih.gov/pubmed/23776359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S13490
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