Cargando…
Digenic mutations on SCAP and AGXT2 predispose to premature myocardial infarction
Genetic factors play a vital role in the pathogenesis of premature myocardial infarction (PMI). However, current studies explained only small amounts of genetic risk in MI. In this study, we started from a PMI pedigree with three MI patients occurred at the age of 43, 45 and 53 respectively. Sanger...
Autores principales: | Gao, Yuanfeng, Lee, Chongyou, Song, Junxian, Li, Sufang, Cui, Yuxia, Liu, Yongzhen, Wang, Jie, Lu, Fengmin, Chen, Hong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725008/ https://www.ncbi.nlm.nih.gov/pubmed/29245966 http://dx.doi.org/10.18632/oncotarget.22045 |
Ejemplares similares
-
Prevalence of familial hypercholesterolemia in patients with premature myocardial infarction
por: Cui, Yuxia, et al.
Publicado: (2019) -
Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction
por: Lee, Chongyou, et al.
Publicado: (2019) -
Prothrombin G20210A (rs1799963) polymorphism increases myocardial infarction risk in an age-related manner: A systematic review and meta-analysis
por: Li, Changlong, et al.
Publicado: (2017) -
ENAM mutations and digenic inheritance
por: Zhang, Hong, et al.
Publicado: (2019) -
Understanding mutational effects in digenic diseases
por: Gazzo, Andrea, et al.
Publicado: (2017)