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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...

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Podrobná bibliografie
Vydáno v:J Cardiovasc Thorac Res
Hlavní autoři: Kalayinia, Samira, Ghasemi, Serwa, Mahdieh, Nejat
Médium: Artigo
Jazyk:Inglês
Vydáno: Tabriz University of Medical Sciences 2019
Témata:
On-line přístup: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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