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Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population
Background: Congenital heart disease (CHD) is the most common birth abnormality, especially for sporadic CHD. However, the etiology of sporadic CHD is largely unknown. NKX2-5, the earliest sign of cardiac progenitor cell differentiation, plays a key role in cardiac morphogenesis, and the mutation of...
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| Опубликовано в: : | Int J Clin Exp Pathol |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
e-Century Publishing Corporation
2015
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4713608/ https://ncbi.nlm.nih.gov/pubmed/26823822 |
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