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Identification of the hyaluronic acid pathway as a therapeutic target for facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is linked to epigenetic derepression of the germline/embryonic transcription factor DUX4 in skeletal muscle. However, the etiology of muscle pathology is not fully understood, as DUX4 misexpression is not tightly correlated with disease severity. Using a...
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| Publicado en: | Sci Adv |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Association for the Advancement of Science
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6905861/ https://ncbi.nlm.nih.gov/pubmed/31844661 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/sciadv.aaw7099 |
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