| 1 | TMEM43, ARVD5 |
| Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. | |
| Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL. | |
| Am J Hum Genet 82(4):809-21. Epub 2008 Feb 28. 2008 | |
| 2 | ARVD5, ARVDPPK |
| Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23. | |
| Ahmad F, et al. | |
| Circulation 98(25):2791-5. 1998 | |