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Novel and Functional DNA Sequence Variants within the GATA6 Gene Promoter in Ventricular Septal Defects
Congenital heart disease (CHD) is the most common birth defect in humans. Genetic causes and underlying molecular mechanisms for isolated CHD remain largely unknown. Studies have demonstrated that GATA transcription factor 6 (GATA6) plays an essential role in the heart development. Mutations in GATA...
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| Autores principales: | , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2014
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4139867/ https://ncbi.nlm.nih.gov/pubmed/25036032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms150712677 |
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