A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
We have previously shown in a large X-linked pedigree that a deletion removing the dystrophin muscle promoter, the first muscle exon and part of intron 1 caused a severe dilated cardiomyopathy with no associated muscle weakness. Dystrophin expression was present in the muscle of affected males and t...
Zapisane w:
| Wydane w: | J Clin Invest |
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| Główni autorzy: | , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
American Society for Clinical Investigation
1995
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC185251/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7635962/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI118112 |
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