The 5′ Region of Intron 11 of the Dystrophin Gene Contains Target Sequences for Mobile Elements and Three Overlapping ORFs
- 1 January 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 242 (2) , 401-406
- https://doi.org/10.1006/bbrc.1997.7976
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Evidence for a Dystrophin Missense Mutation as a Cause of X-Linked Dilated CardiomyopathyCirculation, 1997
- A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated CardiomyopathyHuman Molecular Genetics, 1996
- A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intronHuman Genetics, 1994
- Searching for the 1 in 2,400,000: A review of dystrophin gene point mutationsHuman Mutation, 1994
- Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathyMuscle & Nerve, 1993
- Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated CardiomyopathyNew England Journal of Medicine, 1993
- A Cluster of Transposon-like Repetitive Sequences in Intron 7 of the Human Dystrophin GeneJournal of Molecular Biology, 1993
- X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.Circulation, 1993
- The structural and functional diversity of dystrophinNature Genetics, 1993
- An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locusGenomics, 1988