| 1 | TNNT2, CMD1D
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| Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype.
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| Mirza M, Marston S, Willott R, Ashley C, Mogensen J, McKenna W, Robinson P, Redwood C, Watkins H.
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| J Biol Chem 280(31):28498-506. Epub 2005 May 27. 2005
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| 2 | TNNT2, CMD1D, CMH2
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| The role of a common TNNT2 polymorphism in cardiac hypertrophy.
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| Komamura K, Iwai N, Kokame K, Yasumura Y, Kim J, Yamagishi M, Morisaki T, Kimura A, Tomoike H, Kitakaze M, Miyatake K.
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| J Hum Genet 49(3):129-33. Epub 2004 Feb 24. 2004
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| 3 | TNNT2, CMD1D
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| Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy.
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| Li D, Czernuszewicz GZ, Gonzalez O, Tapscott T, Karibe A, Durand JB, Brugada R, Hill R, Gregoritch JM, Anderson JL, Quinones M, Bachinski LL, Roberts R.
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| Circulation 104(18):2188-93. 2001
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| 4 | CMD1D
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| Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.
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| Durand JB, Bachinski LL, Bieling LC, Czernuszewicz GZ, Abchee AB, Yu QT,Tapscott T, Hill R, Ifegwu J, Marian AJ, et al.
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| Circulation 92(12):3387-9. 1995
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