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New Approaches in Detection and Treatment of Familial Hypercholesterolemia
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder that clinically leads to increased low density lipoprotein-cholesterol (LDL-C) levels. As a consequence, FH patients are at high risk for cardiovascular disease (CVD). Mutations are found in genes coding for the LDLR, apoB,...
Guardat en:
| Publicat a: | Curr Cardiol Rep |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer US
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4611021/ https://ncbi.nlm.nih.gov/pubmed/26482752 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11886-015-0665-x |
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