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11. X-linked dilated cardiomyopathy with a large hot-spot deletion in the dystrophin gene. Tasaki N; Yoshida K; Haruta SI; Kouno H; Ichinose H; Fujimoto Y; Urasawa N; Kawakami T; Taniguchi M; Kurushima S; Shimakura T Intern Med; 2001 Dec; 40(12):1215-21. PubMed ID: 11813847 [TBL] [Abstract][Full Text] [Related]
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13. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy. Muntoni F; Di Lenarda A; Porcu M; Sinagra G; Mateddu A; Marrosu G; Ferlini A; Cau M; Milasin J; Melis MA; Marrosu MG; Cianchetti C; Sanna A; Falaschi A; Camerini F; Giacca M; Mestroni L Heart; 1997 Dec; 78(6):608-12. PubMed ID: 9470882 [TBL] [Abstract][Full Text] [Related]
14. Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy. Muntoni F; Melis MA; Ganau A; Dubowitz V Am J Hum Genet; 1995 Jan; 56(1):151-7. PubMed ID: 7825571 [TBL] [Abstract][Full Text] [Related]
15. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Ortiz-Lopez R; Li H; Su J; Goytia V; Towbin JA Circulation; 1997 May; 95(10):2434-40. PubMed ID: 9170407 [TBL] [Abstract][Full Text] [Related]
16. Molecular genetics of dilated cardiomyopathy. Mestroni L; Krajinovic M; Severini GM; Falaschi A; Giacca M; Camerini F Herz; 1994 Apr; 19(2):97-104. PubMed ID: 8194838 [TBL] [Abstract][Full Text] [Related]
17. A novel muscle-specific enhancer identified within the deletion overlap region of two XLDC patients lacking muscle exon 1 of the human dystrophin gene. Bastianutto C; De Visser M; Muntoni F; Klamut HJ; Patarnello T Genomics; 2002 Dec; 80(6):614-20. PubMed ID: 12504853 [TBL] [Abstract][Full Text] [Related]