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Functional analysis of the congenital heart disease-associated GATA4 H436Y mutation in vitro
Congenital heart disease (CHD) is the most common type of developmental defect, with high rates of morbidity in infants. The transcription factor GATA-binding factor 4 (GATA4) has been reported to serve a critical role in embryogenesis and cardiac development. Our previous study reported a heterozyg...
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| Pubblicato in: | Mol Med Rep |
|---|---|
| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
D.A. Spandidos
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6691264/ https://ncbi.nlm.nih.gov/pubmed/31322241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.10481 |
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