1THIENE G, NAVA A, CORRADO D, et al. Right ventricular cardiomyopathy and sudden death in young people[J]. N Engl J Med,1988,318: 129--133.
2TISO N, STEPHAN D A, NAVA A, et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 ( ARVD2 )[J].Hum Mol Genet, 2001,0 : 189-- 194.
3COONAR A S, PROTONOTARIOS N, TSATSO- POULOU A, et al. Gene for arrhythmogenic right ventricular eardiomyopathy with diffuse nonepidermo lytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21[J]. Circulation, 1998,97:2049--2058.
4MCKOY G, PROTONOTARIOS N, CROSBY A, et al. Identi-fication of a deletion in plakoglobin in ar rhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos dis ease)[J].Lancet ,2000,355:2119--2124.
5RAMPAZZO A, NAVA A, MALACRIDA S, et al. Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy[J]. Am J Hum Genet,2002,71 : 1200-- 1206.
6GERULL B, HEUSER A, WICHTER T, et al. Mutations in the desmosomal protein plakophilin-2 are eommon in arrhythmogenic right ventricular cardiomyopathy[J]. Nat Genet,2004,36:1162- 1164.
7VAN TINTELEN J P, ENTIUS M M, BHUIYAN Z A, et al. Plakophilin 2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy[J].Circulation, 2006, 13: 1650--1658.
8PILICHOU K, NAVA A, BASSO C, et al. Mutations in desmoglein-2 gene are associated with ar rhythmogenic right ventricular cardiomyopathy [J]. Circulation, 2006,113 : 1171 - 1179.
9HEUSER A, PLOVIE E R, ELLINOR P T, et al. Mutant desmocollin-2 causes arrhythmogenic right ventrieular cardiomyopathy[J]. Am J Hum Genet, 2006, 79: 1081--1088.
10SYRRIS P, WARD D, EVANS A, et al. Arrhyth mogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2[J]. Am J Hum Genet, 2006,79 : 978 -- 984.
