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A TBX5 3′UTR variant increases the risk of congenital heart disease in the Han Chinese population
TBX5 is a vital transcription factor involved in cardiac development in a dosage-dependent manner. But little is known about the potential association of TBX5 3′ untranslated region (UTR) variations with congenital cardiac malformations. This study aimed to investigate the relationship between TBX5...
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| Publicat a: | Cell Discov |
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| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5527299/ https://ncbi.nlm.nih.gov/pubmed/28761722 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/celldisc.2017.26 |
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