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An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway
Cyanotic congenital heart disease (CCHD), a term describing the most severe congenital heart diseases are characterized by the anatomic malformation of a right to left shunt. Although the incidence of CCHD are far less than the that of congenital heart diseases (CHD), patients with CCHD always prese...
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| Published in: | Genes Dis |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Chongqing Medical University
2018
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6411777/ https://ncbi.nlm.nih.gov/pubmed/30906831 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2018.03.003 |
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