1Bravennan AC, GUven H, Beardslee MA, et al. The bicuspid aortic valve. Curr Probl Cardiol,2005,30(9) :470-522.
2Aboulhosn J,Child JS.Left ventricular outflow obstruction:subaortic stenosis,bicuspid aortic valve, supravalvar aortic stenosis, and coarctation of the aorta. Circulation, 2006,114(22) : 2412-2422.
3Mack G, Silberbach M. Aortic and pulmonary stenosis. Pediatr Rev, 2000, 21(3) :79-85.
4Andelfinger G, Tapper AR, Welch RC, et al. KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes. Am J Hum Genet,2002,71 (3) :663-668.
5Garg V. Molecular genetics of aortic valve disease. Curr Opin Cardiol, 2006,21 (3) : 180-184.
6Garg V, Muth AN, Ransom JF, et al. Mutations in NOTCH1 cause aortic valve disease. Nature, 2005,437 ( 7056 ) : 270-274.
7Mohamed SA,Aherrahrou Z,Liptau H,et al. Novel missense mutations (p. T596M and p. P1797H) in NOTCH1 in patients with bicuspid aortic valve. Biochem Biophys Res Commun,2006,345(4) : 1460-1465.
8McKellar SH, Tester DJ, Yagubyan M, et al. Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms. J Thorac Cardiovasc Surg,2007,134(2) :290-296.
9Lee TC, Zhao YD, Cenrtman DW, et al. Abnormal aortic valve development in mice lacking endothelial nitric oxide synthase. Circulation, 2000, 101 (20) :2345-2348.
10Aicher D, Urbich C, Zeiher A, et al. Endothelial nitric oxide synthase in bicuspid aortic valve disease. Ann Thorac Surg,2007,83(4) : 1290-1294.