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DUX4 Signalling in the Pathogenesis of Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is a disabling inherited muscular disorder characterized by asymmetric, progressive muscle weakness and degeneration. Patients display widely variable disease onset and severity, and sometimes present with extra-muscular symptoms. There is a consensus th...
Tallennettuna:
| Julkaisussa: | Int J Mol Sci |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7037115/ https://ncbi.nlm.nih.gov/pubmed/31979100 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21030729 |
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