PTPN11 Gene Mutations and Its Association with the Risk of Congenital Heart Disease

Congenital heart disease (CHD) is the most common congenital birth defect, with a prevalence of 8.98‰ of all live births in China. PTPN11 has been known to be closely involved in heart developments. In this research, we carried out whole-exome sequencing in nine CHD families and identified eight rar...

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Detalles Bibliográficos
Autores principales: Xu, Zi-qing, Chen, Wei-cheng, Li, Yu-jie, Suo, Mei-jiao, Tian, Gui-xiang, Sheng, Wei, Huang, Guo-ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013483/
https://www.ncbi.nlm.nih.gov/pubmed/35440950
http://dx.doi.org/10.1155/2022/8290779

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013483/
https://www.ncbi.nlm.nih.gov/pubmed/35440950
http://dx.doi.org/10.1155/2022/8290779

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