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Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation
BACKGROUND: Congenital heart disease (CHD) is a common birth defect, and most cases occur sporadically. Mutations in key genes that are responsible for cardiac development could contribute to CHD. To date, the genetic causes of CHD remain largely unknown. METHODS: In this study, twenty-nine candidat...
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| Veröffentlicht in: | J Transl Med |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5379520/ https://ncbi.nlm.nih.gov/pubmed/28372585 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12967-017-1173-0 |
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