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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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| Publicado no: | J Transl Med |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | 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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