Atrial septal defect

[1]. Edwin P Kirk, et al. Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. Am J Hum Genet. 2007 Aug;81(2):280-91. [Content Brief]

[2]. Hans Matsson, et al. Alpha-cardiac actin mutations produce atrial septal defects. Hum Mol Genet. 2008 Jan 15;17(2):256-65. [Content Brief]

[3]. J J Schott, et al. Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science. 1998 Jul 3;281(5373):108-11. [Content Brief]

[4]. Maximilian G Posch, et al. Molecular genetics of congenital atrial septal defects. Clin Res Cardiol. 2010 Mar;99(3):137-47. [Content Brief]

[5]. Paweł Stańczak, et al. Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD. Eur J Hum Genet. 2009 Mar;17(3):344-51. [Content Brief]

[6]. Silke Sperling, et al. Identification and functional analysis of CITED2 mutations in patients with congenital heart defects. Hum Mutat. 2005 Dec;26(6):575-82. [Content Brief]

[7]. Vidu Garg, et al. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature. 2003 Jul 24;424(6947):443-7. [Content Brief]

[8]. Xiaoping Lin, et al. A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect. J Hum Genet. 2010 Oct;55(10):662-7. [Content Brief]

[9]. Yung-Hao Ching, et al. Mutation in myosin heavy chain 6 causes atrial septal defect. Nat Genet. 2005 Apr;37(4):423-8. [Content Brief]