Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update
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| Author: | Teresa Schätzl, Lars Kaiser, Hans-Peter DeignerORCiDGND |
|---|---|
| URN: | https://urn:nbn:de:bsz:fn1-opus4-71916 |
| DOI: | https://doi.org/10.1186/s13023-021-01760-1 |
| ISSN: | 1750-1172 |
| Parent Title (English): | Orphanet Journal of Rare Diseases |
| Document Type: | Article (peer-reviewed) |
| Language: | English |
| Year of Completion: | 2021 |
| Release Date: | 2021/04/12 |
| Tag: | Double Homeobox 4 (DUX4); Downstream signalling; Epigenetic; Facioscapulohumeral muscular dystrophy (FSHD); Treatment strategies |
| Volume: | 16.2021 |
| Issue: | Artikel 129 |
| Page Number: | 26 |
| Open-Access-Status: | Open Access |
| Licence (German): |  Creative Commons - CC BY - Namensnennung 4.0 International |