DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model
Myotonic dystrophy (DM) is the most common form of muscular dystrophy and is caused by expansion of a CTG trinucleotide repeat on human chromosome 19. Patients with DM develop atrioventricular conduction disturbances, the principal cardiac manifestation of this disease. The etiology of the pathophys...
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
1999
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC408103/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10021468/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI5346 |
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