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Lack of association between the APLNR variant rs9943582 with ischemic stroke in the Chinese Han GeneID population
Stroke is one of the most common causes of death worldwide. Genetic risk factors have been found to play important roles in the pathology of ischemic stroke. In a previous genome-wide association study, a functional variant (rs9943582, –154G/A) in the 5’ flanking region of the apelin receptor gene (...
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| Publicat a: | Oncotarget |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Impact Journals LLC
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5746099/ https://ncbi.nlm.nih.gov/pubmed/29296197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.22588 |
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