1Coumel P, Fidelle J, Lucet V, et al. Catecholaminergic induced severe ventricular arrhythmias with Adams-Stokes syndrome in children: report of four cases[J]. Br Heart J,1978,40(1):28- 37.
2Leenhardt A, Lucet V, Denjoy I, et al. Catecholaminergic polymorphic ventricular tachycardia in children. A 7 year follow- up of 21 patients[J]. Circulation,1995,91(5):1512-1519.
3Laitinen P J, Brown K M, Piippo K, et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia[J]. Circulation,2001,103(4):485-490.
4Marks A R, Priori S, Memmi M, et al. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia[J]. J Cell Physiol,2002,190(1): 1-6.
5Lahat H, Pras E, Olender T, et al. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine induced polymorphic ventricular tachycardia in Bedouin families from Israel [J]. Am J Hum Genet,2001, 69(6) :1378-1384.
6Postma A V, Denjoy I, Hoorntje T M, et al. Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia[J]. Circ Res, 2002,91 (8):e21-e26.
7Priori S G, Napolitano C, Memmi M, et al. Clinical and molecular characterization of patients with catecholaminergie polymorphic ventricular tachycardia [J]. Circulation, 2002, 106 (1):69-74.
