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Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction
Myocardial infarction (MI), a leading cause of death around the world, displays a complex pattern of inheritance(1,2). When MI occurs early in life, the role of inheritance is substantially greater(1). Previously, rare mutations in low-density lipoprotein (LDL) genes have been shown to contribute to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319990/ https://www.ncbi.nlm.nih.gov/pubmed/25487149 http://dx.doi.org/10.1038/nature13917 |