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Identification of epigenetic factor KAT2B gene variants for possible roles in congenital heart diseases
Congenital heart disease (CHD) is a group of anatomic malformations in the heart with high morbidity and mortality. The mammalian heart is a complex organ, the formation and development of which are strictly regulated and controlled by gene regulatory networks of many signaling pathways such as TGF-...
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| Publicado no: | Biosci Rep |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Portland Press Ltd.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7160239/ https://ncbi.nlm.nih.gov/pubmed/32239175 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20191779 |
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