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Challenges in the Diagnosis and Treatment of Homozygous Familial Hypercholesterolemia
Homozygous familial hypercholesterolemia (HoFH) is a rare, genetic disorder characterized by an absence or impairment of low-density lipoprotein receptor (LDLR) function resulting in significantly elevated low-density lipoprotein cholesterol (LDL-C) levels. The cholesterol exposure burden beginning...
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| Publicado en: | Drugs |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Springer International Publishing
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4611011/ https://ncbi.nlm.nih.gov/pubmed/26370207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40265-015-0466-y |
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