| 1 | CMD1M, CSRP3
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| Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
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| Geier C, Gehmlich K, Ehler E, Hassfeld S, Perrot A, Hayess K, Cardim N, Wenzel K, Erdmann B, Krackhardt F, Posch MG, Bublak A, Nägele H, Scheffold T, Dietz R, Chien KR, Spuler S, Fürst DO, Nürnberg P, Ozcelik C.
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| Hum Mol Genet 17(18):2753-65. Epub 2008 May 27.
2008
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| 2 | ACTN2, CMD1M, CSRP3
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| Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.
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| Mohapatra B, Jimenez S, Lin JH, Bowles KR, Coveler KJ, Marx JG, Chrisco MA, Murphy RT, Lurie PR, Schwartz RJ, Elliott PM, Vatta M, McKenna W, Towbin JA, Bowles NE.
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| Mol Genet Metab 80(1-2):207-15. 2003
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| 3 | CSRP3, CMD1M
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| Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
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| Geier C, Perrot A, Ozcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, Martiniak Y, Gehmlich K, van der Ven PF, Furst DO, Vornwald A, von Hodenberg E, Nurnberg P, Scheffold T, Dietz R, Osterziel KJ.
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| Circulation 107(10):1390-5. 2003
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| 4 | CMD1M, CSRP3, TCAP
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| The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy.
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| Knoll R, Hoshijima M, Hoffman HM, Person V, Lorenzen-Schmidt I, Bang ML, Hayashi T, Shiga N, Yasukawa H, Schaper W, McKenna W, Yokoyama M, Schork NJ, Omens JH, McCulloch AD, Kimura A, Gregorio CC, Poller W, Schaper J, Schultheiss HP, Chien KR.
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| Cell 111(7):943-55. 2002
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