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Straightjacket/α2δ3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1
Cardiac conduction defects decrease life expectancy in myotonic dystrophy type 1 (DM1), a CTG repeat disorder involving misbalance between two RNA binding factors, MBNL1 and CELF1. However, how DM1 condition translates into conduction disorders remains poorly understood. Here we simulated MBNL1 and...
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| Publicado no: | eLife |
|---|---|
| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
eLife Sciences Publications, Ltd
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6908436/ https://ncbi.nlm.nih.gov/pubmed/31829940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.51114 |
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