A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus
Author:
Affiliation:
1. Fudan University, China
2. Fudan University, China; Fudan University, China
3. Shanghai Jiao Tong University, China
4. Fudan University, China; Fudan University, China; Fudan University, China; Fudan University, China
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v45n2/1415-4757-GMB-45-2-e20210378.pdf
Reference70 articles.
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3. Loss of function of the Prx1 and Prx2 homeobox genes alters architecture of the great elastic arteries and ductus arteriosus;Bergwerff M;Virchows Arch,2000
4. Targeted mutation reveals essential functions of the homeodomain transcription factor SHOX2 in sinoatrial and pacemaking development;Blaschke RJ;Circulation,2007
5. A variant noncoding region regulates PRRX1 and predisposes to atrial arrhythmias;Bosada FM;Circ Res,2021
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