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Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects
Introduction: Congenital heart diseases (CHDs) are structural cardiovascular malformations that arise from abnormal development of the heart during the prenatal life. Mutations in the TBX5 gene, encoding T-box transcription factor, are a major cause of CHD. To evaluate the TBX5 mutations in hotspot...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Tabriz University of Medical Sciences
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913692/ https://www.ncbi.nlm.nih.gov/pubmed/29707177 http://dx.doi.org/10.15171/jcvtr.2018.07 |