Ostium Secundum Atrial Septal Defect
What's New
Last Posted: Mar 06, 2023
- Identification of LBX2 as a novel causal gene of atrial septal defect.
Wang Jing, et al. International journal of cardiology 2018 0 188-194 - Association Between the 4p16 Susceptibility Locus and the Risk of Atrial Septal Defect in Population from Southeast China.
Pei Kaiyan, et al. Pediatric cardiology 2015 8 - Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot.
Baban Anwar, et al. American journal of medical genetics. Part A 2014 12 (12) 3100-7 - Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations.
Zhao Bijun, et al. PloS one 2014 0 (9) e107411 - Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Cordell Heather J, et al. Nature genetics 2013 7 (7) 822-4 - Ostium secundum atrial septal defect
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