Citations for
1CMD1N, GATA4
GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
Li RG, Li L, Qiu XB, Yuan F, Xu L, Li X, Xu YJ, Jiang WF, Jiang JQ, Liu X, Fang WY, Zhang M, Peng LY, Qu XK, Yang YQ.
Biochem Biophys Res Commun 439(4):591-6. doi: 10.1016/j.bbrc.2013.09.023. Epub 2013 Sep 13. 2013
2CMD1N, TCAP
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M.
Clin Transl Sci 1(1):21-26.PMID: 19412328 2008
3CMD1N, MYOZ2, TCAP
Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.
Hayashi T, Arimura T, Itoh-Satoh M, Ueda K, Hohda S, Inagaki N, Takahashi M, Hori H, Yasunami M, Nishi H, Koga Y, Nakamura H, Matsuzaki M, Choi BY, Bae SW, You CW, Han KH, Park JE, Knoll R, Hoshijima M, Chien KR, Kimura A.
J Am Coll Cardiol 44(11):2192-201. 2004