| 1 | CMD1C, LDB3
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| Combination of Genetic Screening and Molecular Dynamics as a Useful Tool for Identification of Disease-Related Mutations: ZASP PDZ Domain G54S Mutation Case.
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| Fratev F, Mihaylova E, Pajeva I.
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| J Chem Inf Model 54(5):1524-36. doi: 10.1021/ci5001136. Epub 2014 Apr 28.
2014
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| 2 | CMD1C, LDB3
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| Cardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death.
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| Zheng M, Cheng H, Li X, Zhang J, Cui L, Ouyang K, Han L, Zhao T, Gu Y, Dalton ND, Bang ML, Peterson KL, Chen J.
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| Hum Mol Genet 18(4):701-13. Epub 2008 Nov 21.
2009
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| 3 | CMD1C, LDB3
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| A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.
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| Arimura T, Hayashi T, Terada H, Lee SY, Zhou Q, Takahashi M, Ueda K, Nouchi T, Hohda S, Shibutani M, Hirose M, Chen J, Park JE, Yasunami M, Hayashi H, Kimura A.
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| J Biol Chem 279(8):6746-52. Epub 2003 Dec 3. 2004
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| 4 | ARVD7, CMD1C, POLR3A, PPIF
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| Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes.
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| Bowles KR, Abraham SE, Brugada R, Zintz C, Comeaux J, Sorajja D, Tsubata S, Li H, Brandon L, Gibbs RA, Scherer SE, Bowles NE, Towbin JA.
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| Genomics 67(2):109-27. 2000
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| 5 | CMD1C
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| Genetic linkage of autosomal dominant dilated cardiomyopathy and limb-girdle muscular dystrophy. (abstr)
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| McNally EM, et al.
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| Am J Hum Genet 61 : A29. 1997
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| 6 | CMD1C
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| Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
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| Bowles KR, et al.
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| J Clin Invest 98 : 1355-1360. 1996
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