| 1 | CMD3B
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| Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.
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| Franz WM, Muller M, Muller OJ, Herrmann R, Rothmann T, Cremer M, Cohn RD, Voit T, Katus HA.
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| Lancet 355(9217):1781-5. 2000
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| 2 | CMD3B
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| X-linked dilated cardiomyopathy and the dystrophin gene.
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| Ferlini A, et al.
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| Neuromuscul Disord 9(5):339-46. Review 1999
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| 3 | CMD3B, DMD
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| Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.
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| Yoshida K, et al.
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| Hum Mol Genet 7 : 1129-1132. 1998
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| 4 | CMD3B, DMD
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| A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.
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| Ferlini A, et al.
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| Am J Hum Genet 63 : 436-446. 1998
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| 5 | CMD3B, DMD
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| Study on mutations affecting the muscle promoter/first exon of the dystrophin gene in 92 Japanese dilated cardiomyopathy patients.
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| Shiga N, et al.
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| Am J Med Genet 79 : 226-227. 1998
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| 6 | CMD3B
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| Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.
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| Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA.
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| Circulation 95(10):2434-40. 1997
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| 7 | CMD3B, DMD
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| A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.
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| Bies RD, Maeda M, Roberds SL, Holder E, Bohlmeyer T, Young JB, Campbell KP.
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| J Mol Cell Cardiol 29(12):3175-88. 1997
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| 8 | CMD3B, DMD
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| A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.
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| Milasin J, et al.
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| Hum Mol Genet 5 : 73-79. 1996
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| 9 | CMD3B, DMD
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| A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
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| Muntoni F, et al.
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| J Clin Invest 96 : 693-699. 1995
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| 10 | CMD3B, DMD
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| Mutation of dystrophin gene and cardiomyopathy.
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| Nigro G, et al.
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| Neuromuscul Disord 4 : 371-379. 1994
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| 11 | CMD3B
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| Dystrophin analysis in idiopathic dilated cardiomyopathy.
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| Michels VV, et al.
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| J Med Genet 30 : 955-957. 1993
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| 12 | CMD3B
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| X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
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| Towbin JA, et al.
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| Circulation 87 : 1854-1865. 1993
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| 13 | CMD3B
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| Brief report : deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.
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| Muntoni F, et al.
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| N Engl J Med 329 : 921-925. 1993
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| 14 | CMD3B
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| X-linked dilated cardiomyopathy (XLCM) : molecular characterization.
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| Towbin JA, et al.
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| Am J Hum Genet 49 : 421. 1991
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