Cargando…
A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction
BACKGROUND: Myocardial infarction (MI) is a multifactorial disease caused by the suspension of blood circulation in a part of the myocardium. Understanding the genetic basis of MI can provide insight regarding the pathogenesis of the disease. The aim of this study was to investigate the association...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172235/ https://www.ncbi.nlm.nih.gov/pubmed/34122585 http://dx.doi.org/10.22122/arya.v16i6.1797 |