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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...
Tallennettuna:
| Julkaisussa: | Cell Discov |
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| Päätekijät: | , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Nature Publishing Group
2017
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| Aiheet: | |
| Linkit: | 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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