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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...
Kaydedildi:
| Yayımlandı: | Int J Clin Exp Pathol |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
e-Century Publishing Corporation
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4713608/ https://ncbi.nlm.nih.gov/pubmed/26823822 |
| Etiketler: |
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