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Mouse model of severe recessive RYR1-related myopathy
Ryanodine receptor type I (RYR1)-related myopathies (RYR1 RM) are a clinically and histopathologically heterogeneous group of conditions that represent the most common subtype of childhood onset non-dystrophic muscle disorders. There are no treatments for this severe group of diseases. A major barri...
Gardado en:
| Publicado en: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6737254/ https://ncbi.nlm.nih.gov/pubmed/31107960 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz105 |
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