Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease
Abstract Objective Coronary artery disease contributes to noncommunicable disease deaths worldwide. In order to make preventive methods more accurate, we need to know more about the development and progress of this pathology, including the genetic aspects. Humanin is a small peptide known for its cy...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2019-11-01
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| Edice: | BMC Research Notes |
| Témata: | |
| On-line přístup: | http://link.springer.com/article/10.1186/s13104-019-4807-x |
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