Yüklüyor......
A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease
Introduction: Congenital heart disease (CHD) affects 1% to 2 % of live births. The Nkx2-5 gene, is known as the significant heart marker during embryonic evolution and it is also necessary for the survival of cardiomyocytes and homeostasis in adulthood. In this study, Nkx2-5 mutations are investigat...
Kaydedildi:
| Yayımlandı: | J Cardiovasc Thorac Res |
|---|---|
| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Tabriz University of Medical Sciences
2019
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6891041/ https://ncbi.nlm.nih.gov/pubmed/31824610 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15171/jcvtr.2019.47 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|