A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve

Recently, mutations in the Kruppel-like factor 13 (KLF13) gene encoding a Kruppel-like transcription factor have been reported to cause congenital heart disease (CHD). However, due to pronounced genetic heterogeneity, the mutational spectrum of KLF13 in other cohorts of cases suffering from distinct...

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Detalles Bibliográficos
Autores principales: Abhinav, Pradhan, Zhang, Gao-Feng, Zhao, Cui-Mei, Xu, Ying-Jia, Wang, Juan, Yang, Yi-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943534/
https://www.ncbi.nlm.nih.gov/pubmed/35369534
http://dx.doi.org/10.3892/etm.2022.11240

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943534/
https://www.ncbi.nlm.nih.gov/pubmed/35369534
http://dx.doi.org/10.3892/etm.2022.11240

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