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Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia
BACKGROUND: Familial hypercholesterolemia (FH) is an autosomal-dominant disease leading to markedly elevated low-density lipoprotein (LDL) cholesterol levels and increased risk for premature myocardial infarction (MI). Mutation carriers display variable LDL cholesterol levels, which may obscure the...
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| Publicat a: | BMC Cardiovasc Disord |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4243586/ https://ncbi.nlm.nih.gov/pubmed/25154303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2261-14-108 |
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