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Identification of drug modifiers for RYR1-related myopathy using a multi-species discovery pipeline
Ryanodine receptor type I-related myopathies (RYR1-RMs) are a common group of childhood muscle diseases associated with severe disabilities and early mortality for which there are no available treatments. The goal of this study is to identify new therapeutic targets for RYR1-RMs. To accomplish this,...
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| Publicado no: | eLife |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
eLife Sciences Publications, Ltd
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7202896/ https://ncbi.nlm.nih.gov/pubmed/32223895 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.52946 |
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