1Schwartz PJ, Moss AJ, Vincent GM,et al. Diagnostic criteria for the long QT syndrome: an update. Circulation, 1993, 88:782-784. 被引量:1
2Trippel DL, Parsons MK, Gillette PC. Infants with long-QT syndrome and 2: 1 atrioventricular block. Am Heart J, 1995, 130: 1130-1134. 被引量:1
3Moss AJ, Zareba W, Benhorin J, et al. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation, 1995, 92:2929-2934. 被引量:1
4Pruvot E, De Torrente A, De Ferrari GM, et al. Two-to-one AV block associated with the congenital long QT syndrome. J Cardiovasc Electrophysiol, 1999, 10: 108-113. 被引量:1
5Piipo K, Laitinen P, Swan H,et al. Homozygosity for HERG potassium channel mutation causes a severe from of long QT syndrome: identification of an apparent founder mutation in Finns. J Am Coll Cardiol, 2000, 35: 1264-1267. 被引量:1
6Lupoglazoff JM, Cheav T, Baroudi G, et al. Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block. Circ Res, 2001, 89:16. 被引量:1