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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Detalles Bibliográficos
Autores principales: Li, Chunyu, Li, Xianke, Pang, Shuchao, Chen, Wei, Qin, Xianyun, Huang, Wenhui, Zeng, Changqing, Yan, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139867/
https://www.ncbi.nlm.nih.gov/pubmed/25036032
http://dx.doi.org/10.3390/ijms150712677

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139867/
https://www.ncbi.nlm.nih.gov/pubmed/25036032
http://dx.doi.org/10.3390/ijms150712677

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