These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
134 related articles for article (PubMed ID: 12794683)
1. Dilated cardiomyopathy and new 16 bp deletion in exon 44 of the Dystrophin gene: the possible role of repeated motifs in mutation generation. Todorova A; Constantinova D; Kremensky I Am J Med Genet A; 2003 Jul; 120A(1):5-7. PubMed ID: 12794683 [TBL] [Abstract][Full Text] [Related]
2. Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for x-linked dilated cardiomyopathy. Rimessi P; Fabris M; Bovolenta M; Bassi E; Falzarano S; Gualandi F; Rapezzi C; Coccolo F; Perrone D; Medici A; Ferlini A Hum Gene Ther; 2010 Sep; 21(9):1137-46. PubMed ID: 20486769 [TBL] [Abstract][Full Text] [Related]
3. Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27. Tsuda T; Fitzgerald K; Scavena M; Gidding S; Cox MO; Marks H; Flanigan KM; Moore SA J Hum Genet; 2015 Mar; 60(3):151-5. PubMed ID: 25537791 [TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy. Yoshida K; Ikeda S; Nakamura A; Kagoshima M; Takeda S; Shoji S; Yanagisawa N Muscle Nerve; 1993 Nov; 16(11):1161-6. PubMed ID: 8413368 [TBL] [Abstract][Full Text] [Related]
5. Dilated cardiomyopathy and the dystrophin gene: an illustrated review. Oldfors A; Eriksson BO; Kyllerman M; Martinsson T; Wahlström J Br Heart J; 1994 Oct; 72(4):344-8. PubMed ID: 7833192 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Towbin JA; Hejtmancik JF; Brink P; Gelb B; Zhu XM; Chamberlain JS; McCabe ER; Swift M Circulation; 1993 Jun; 87(6):1854-65. PubMed ID: 8504498 [TBL] [Abstract][Full Text] [Related]
8. Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy. Feng J; Yan J; Buzin CH; Towbin JA; Sommer SS Mol Genet Metab; 2002; 77(1-2):119-26. PubMed ID: 12359139 [TBL] [Abstract][Full Text] [Related]
9. Dilated cardiomyopathy of Becker-type muscular dystrophy with exon 4 deletion--a case report. Saotome M; Yoshitomi Y; Kojima S; Kuramochi M Angiology; 2001 May; 52(5):343-7. PubMed ID: 11386386 [TBL] [Abstract][Full Text] [Related]
10. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations. Kitoh Y; Matsuo M; Nishio H; Nakamura H Kobe J Med Sci; 1994 Apr; 40(2):39-48. PubMed ID: 7823533 [TBL] [Abstract][Full Text] [Related]
11. Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells. van Deutekom JC; Bremmer-Bout M; Janson AA; Ginjaar IB; Baas F; den Dunnen JT; van Ommen GJ Hum Mol Genet; 2001 Jul; 10(15):1547-54. PubMed ID: 11468272 [TBL] [Abstract][Full Text] [Related]
12. Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophy. Kaspar RW; Allen HD; Ray WC; Alvarez CE; Kissel JT; Pestronk A; Weiss RB; Flanigan KM; Mendell JR; Montanaro F Circ Cardiovasc Genet; 2009 Dec; 2(6):544-51. PubMed ID: 20031633 [TBL] [Abstract][Full Text] [Related]
13. Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy. Narita N; Nishio H; Kitoh Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M J Clin Invest; 1993 May; 91(5):1862-7. PubMed ID: 8387534 [TBL] [Abstract][Full Text] [Related]
14. Novel Rod Domain Duplication in Dystrophin Resulting in X-Linked Dilated Cardiomyopathy. Chamberlain RC; Smith EC; Campbell MJ Pediatr Neurol; 2015 Nov; 53(5):439-41. PubMed ID: 26294044 [TBL] [Abstract][Full Text] [Related]
15. Molecular basis of hypertrophic and dilated cardiomyopathy. Marian AJ; Roberts R Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512 [TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing. Chen WJ; Lin QF; Zhang QJ; He J; Liu XY; Lin MT; Murong SX; Liou CW; Wang N Clin Chim Acta; 2013 Aug; 423():35-8. PubMed ID: 23588064 [TBL] [Abstract][Full Text] [Related]
17. A novel dystrophin deletion mutation in a becker muscular dystrophy patient with early-onset dilated cardiomyopathy. Guo X; Dai Y; Cui L; Fang Q Can J Cardiol; 2014 Aug; 30(8):956.e1-3. PubMed ID: 24996370 [TBL] [Abstract][Full Text] [Related]
18. Rapid direct sequence analysis of the dystrophin gene. Flanigan KM; von Niederhausern A; Dunn DM; Alder J; Mendell JR; Weiss RB Am J Hum Genet; 2003 Apr; 72(4):931-9. PubMed ID: 12632325 [TBL] [Abstract][Full Text] [Related]
19. Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions. Takeshita E; Minami N; Minami K; Suzuki M; Awashima T; Ishiyama A; Komaki H; Nishino I; Sasaki M Neuromuscul Disord; 2017 Jun; 27(6):569-573. PubMed ID: 28434908 [TBL] [Abstract][Full Text] [Related]
20. Becker muscular dystrophy severity is linked to the structure of dystrophin. Nicolas A; Raguénès-Nicol C; Ben Yaou R; Ameziane-Le Hir S; Chéron A; Vié V; Claustres M; Leturcq F; Delalande O; Hubert JF; Tuffery-Giraud S; Giudice E; Le Rumeur E; Hum Mol Genet; 2015 Mar; 24(5):1267-79. PubMed ID: 25348330 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]