| 1 | CMH7, TNNI3
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| Hypertrophic Cardiomyopathy Accompanied by Spinocerebellar Atrophy With a Novel Mutation in Troponin I Gene.
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| Kawai H, Morimoto S, Takakuwa Y, Ueda A, Inada K, Sarai M, Arimura T, Mutoh T, Kimura A, Ozaki Y.
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| Int Heart J 57(4):507-10. doi: 10.1536/ihj.15-444.
2016
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| 2 | CMH7, TNNI3
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| Pediatric restrictive cardiomyopathy due to a heterozygous mutation of the TNNI3 gene.
|
| Chen Y, Yang S, Li J, Wang G, Qin Y, Wang D, Cao K.
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| J Biomed Res 28(1):59-63. doi: 10.7555/JBR.28.20120105.
2014
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| 3 | CMH7, TNNI3
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| Homozygous mutation in the cardiac troponin I gene: clinical heterogeneity in hypertrophic cardiomyopathy.
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| Gray B, Yeates L, Medi C, Ingles J, Semsarian C.
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| Int J Cardiol 168(2):1530-1. doi: 10.1016/j.ijcard.2012.12.008. No abstract available.
2013
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| 4 | TNNI3, CMH7
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| Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy.
|
| Murphy RT, Mogensen J, Shaw A, Kubo T, Hughes S, McKenna WJ.
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| Lancet 363(9406):371-2. 2004
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| 5 | CMH7, TNNI3
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| Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy.
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| Kimura A, Harada H, Park JE, Nishi H, Satoh M, Takahashi M, Hiroi S, Sasaoka T, Ohbuchi N, Nakamura T, Koyanagi T, Hwang TH, Choo JA, Chung KS, Hasegawa A, Nagai R, Okazaki O, Nakamura H, Matsuzaki M, Sakamoto T, Toshima H, Koga Y, Imaizumi T, Sasazuki T.
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| Nat Genet 16(4):379-82. 1997
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