Comprehensive analysis of desmosomal gene mutations in Han Chinese patients with arrhythmogenic right ventricular cardiomyopathy.

[1]  D. Corrado,et al.  Compound and Digenic Heterozygosity Predicts Lifetime Arrhythmic Outcome and Sudden Cardiac Death in Desmosomal Gene–Related Arrhythmogenic Right Ventricular Cardiomyopathy , 2013, Circulation. Cardiovascular genetics.

[2]  R. Hui,et al.  Correlation of Ventricular Arrhythmias With Genotype in Arrhythmogenic Right Ventricular Cardiomyopathy , 2013, Circulation. Cardiovascular genetics.

[3]  K. Sun,et al.  Screening of pathogenic genes in Chinese patients with arrhythmogenic right ventricular cardiomyopathy , 2013, Chinese medical journal.

[4]  M. Horie,et al.  Age-dependent clinical and genetic characteristics in Japanese patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. , 2013, Circulation journal : official journal of the Japanese Circulation Society.

[5]  G. Thiene,et al.  Desmin Mutations and Arrhythmogenic Right Ventricular Cardiomyopathy , 2013, The American journal of cardiology.

[6]  D. Corrado,et al.  Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy. , 2013, European heart journal.

[7]  A. Caro-Vadillo,et al.  Arrhythmogenic right ventricular cardiomyopathy in boxer dogs: a retrospective study of survival , 2013, Veterinary Record.

[8]  R. Hauer,et al.  Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy , 2012, European journal of heart failure.

[9]  M. Kurabayashi,et al.  Compound and digenic heterozygosity in desmosome genes as a cause of arrhythmogenic right ventricular cardiomyopathy in Japanese patients. , 2012, Circulation journal : official journal of the Japanese Circulation Society.

[10]  Brian R. Anderson,et al.  Genetic Variation in Titin in Arrhythmogenic Right Ventricular Cardiomyopathy–Overlap Syndromes , 2011, Circulation.

[11]  R. Hauer,et al.  Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise. , 2011, Journal of the American College of Cardiology.

[12]  P. Nallari,et al.  Novel mutations in arrhythmogenic right ventricular cardiomyopathy from Indian population , 2011, Indian journal of human genetics.

[13]  R. Erbel,et al.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update , 2011, Clinical Research in Cardiology.

[14]  R. Hauer,et al.  Recurrent and founder mutations in the Netherlands , 2010 .

[15]  Wojciech Zareba,et al.  Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: Proposed Modification of the Task Force Criteria , 2010, European heart journal.

[16]  S. Scherer,et al.  Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy. , 2010, Journal of the American College of Cardiology.

[17]  I. V. Van Gelder,et al.  Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene. , 2009, Heart rhythm.

[18]  S. Russell,et al.  Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy , 2009, Circulation. Cardiovascular genetics.

[19]  R. Hauer,et al.  Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study , 2009, Circulation. Cardiovascular genetics.

[20]  Li Zhang,et al.  Mutations of plakophilin-2 in Chinese with arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2009, The American journal of cardiology.

[21]  L. Lai,et al.  Erratum: Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations (Journal of the Formosan Medical Association (2008) vol. 107 (7) (548-558)) , 2009 .

[22]  Z. Shan,et al.  Mutation of plakophilin-2 gene in arrhythmogenic right ventricular cardiomyopathy. , 2009, Chinese medical journal.

[23]  L. Lai,et al.  Arrhythmogenic right ventricular dysplasia: clinical characteristics and identification of novel desmosome gene mutations. , 2008, Journal of the Formosan Medical Association = Taiwan yi zhi.

[24]  Sean Connors,et al.  Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. , 2008, American journal of human genetics.

[25]  Petros Syrris,et al.  Clinical and Genetic Characterization of Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Provides Novel Insights Into Patterns of Disease Expression , 2007, Circulation.

[26]  P. Ellinor,et al.  Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. , 2006, American journal of human genetics.

[27]  P. Syrris,et al.  Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2. , 2006, American journal of human genetics.

[28]  S. Russell,et al.  Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy. , 2006, Journal of the American College of Cardiology.

[29]  M. Horie,et al.  Novel mutation of plakophilin-2 associated with arrhythmogenic right ventricular cardiomyopathy. , 2006, Circulation journal : official journal of the Japanese Circulation Society.

[30]  S. Russell,et al.  Clinical Features of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated With Mutations in Plakophilin-2 , 2006, Circulation.

[31]  R. Hauer,et al.  Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy , 2006, Circulation.

[32]  D. Corrado,et al.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: clinical impact of molecular genetic studies. , 2006, Circulation.

[33]  G. Danieli,et al.  Mutations in Desmoglein-2 Gene Are Associated With Arrhythmogenic Right Ventricular Cardiomyopathy , 2006, Circulation.

[34]  P. Elliott,et al.  Clinical Expression of Plakophilin-2 Mutations in Familial Arrhythmogenic Right Ventricular Cardiomyopathy , 2006, Circulation.

[35]  S. Russell,et al.  Arrhythmogenic Right Ventricular Dysplasia: A United States Experience , 2005, Circulation.

[36]  S. Peters,et al.  Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital. , 2004, International journal of cardiology.

[37]  Walter Birchmeier,et al.  Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy , 2004, Nature Genetics.

[38]  G. Danieli,et al.  Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. , 2002, American journal of human genetics.

[39]  A. Maseri,et al.  Histologic findings in patients with clinical and instrumental diagnosis of sporadic arrhythmogenic right ventricular dysplasia. , 2002, Journal of the American College of Cardiology.

[40]  A. Crosby,et al.  Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease) , 2000, The Lancet.

[41]  M. Davies,et al.  Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. , 1997, Journal of the American College of Cardiology.

[42]  G. Thiene,et al.  Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. , 1994, British heart journal.

[43]  J. Gallagher,et al.  Long-term follow-up in patients with arrhythmogenic right ventricular disease. , 1989, European heart journal.