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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681171/ https://www.ncbi.nlm.nih.gov/pubmed/23776359 http://dx.doi.org/10.2147/TACG.S13490 |