Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.
Author:
Affiliation:
1. Department of Pediatric Cardiology Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China
2. Scientific Research Center Xinhua Hospital School of Medicine Shanghai Jiao Tong University Shanghai China
Funder
Shanghai Municipal Education Commission
National Natural Science Foundation of China
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1771
Reference23 articles.
1. Two Heterozygous Mutations in NFATC1 in a Patient with Tricuspid Atresia
2. Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa
3. Shared gene expression profiles in developing heart valves and osteoblast progenitor cells
4. Transcriptional Regulation of Heart Valve Progenitor Cells
5. NFAT Signaling
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