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Genetic diagnosis of familial hypercholesterolemia is associated with a premature and high coronary heart disease risk
BACKGROUND: Familial hypercholesterolemia (FH) is a common autosomal dominant disease associated with premature coronary heart disease (CHD). Studies tend to show that patients with FH associated with an identified mutation (mutation+ FH) are at higher risk than patients without an identified mutati...
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| Publicado no: | Clin Cardiol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Periodicals, Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6489920/ https://ncbi.nlm.nih.gov/pubmed/29574850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.22881 |
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