1 | CMD1N, GATA4
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| GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
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| 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.
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| Biochem Biophys Res Commun 439(4):591-6. doi: 10.1016/j.bbrc.2013.09.023. Epub 2013 Sep 13.
2013
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2 | CMD1N, TCAP
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| Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
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| Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M.
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| Clin Transl Sci 1(1):21-26.PMID: 19412328 2008
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3 | CMD1N, MYOZ2, TCAP
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| Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.
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| 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.
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| J Am Coll Cardiol 44(11):2192-201. 2004
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