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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...
Gorde:
| Argitaratua izan da: | J Cardiovasc Thorac Res |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Tabriz University of Medical Sciences
2019
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| Gaiak: | |
| Sarrera elektronikoa: | 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 |
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