Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01422.x/fullpdf
Reference25 articles.
1. Genetic basis of congenital heart disease;Gelb;Curr Opin Cardiol,2004
2. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.;Elliott;J Am Coll Cardiol,2003
3. Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene;Gutierrez-Roelens;Hum Mutat,2002
4. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?;Gutierrez-Roelens;Eur J Hum Genet,2006
5. Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.;Ikeda;Circ J,2002
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