| 1 | CMD1KK, MYPN |
| Disturbance in Z-disk mechanosensitive proteins induced by a persistent mutant myopalladin causes familial restrictive cardiomyopathy. | |
| Huby AC, Mendsaikhan U, Takagi K, Martherus R, Wansapura J, Gong N, Osinska H, James JF, Kramer K, Saito K, Robbins J, Khuchua Z, Towbin JA, Purevjav E. | |
| J Am Coll Cardiol 64(25):2765-76. doi: 10.1016/j.jacc.2014.09.071. 2014 | |
| 2 | CMD1KK, MYPN |
| Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. | |
| Purevjav E, Arimura T, Augustin S, Huby AC, Takagi K, Nunoda S, Kearney DL, Taylor MD, Terasaki F, Bos JM, Ommen SR, Shibata H, Takahashi M, Itoh-Satoh M, McKenna WJ, Murphy RT, Labeit S, Yamanaka Y, Machida N, Park JE, Alexander PM, Weintraub RG, Kitaura Y, Ackerman MJ, Kimura A, Towbin JA. | |
| Hum Mol Genet 21(9):2039-53. doi: 10.1093/hmg/dds022. 2012 | |
| 3 | CMD1KK, MYPN |
| Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy. | |
| Duboscq-Bidot L, Xu P, Charron P, Neyroud N, Dilanian G, Millaire A, Bors V, Komajda M, Villard E. | |
| Cardiovasc Res 77(1):118-25. Epub 2007 Sep 19.PMID: 18006477 2008 | |