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...

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Detalhes bibliográficos
Publicado no:ARYA Atheroscler
Main Authors: Ghorbani, Mohammad Javad, Razmi, Nematollah, Tabei, Seyed Mohammad Bagher, Zibaeenezhad, Mohammad Javad, Goodarzi, Hamid Reza
Formato: Artigo
Idioma:Inglês
Publicado em: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2020
Assuntos:
Short Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8172235/
https://ncbi.nlm.nih.gov/pubmed/34122585
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22122/arya.v16i6.1797
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