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A Pediatric Review of Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral dystrophy is one of the most common forms of muscular dystrophies worldwide. It is a complex and heterogeneous disease secondary to insufficient epigenetic repression of D4Z4 repeats and aberrant expression of DUX4 in skeletal muscles. Type 1 facioscapulohumeral muscular dystroph...
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| Gepubliceerd in: | J Pediatr Neurol |
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| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6435288/ https://ncbi.nlm.nih.gov/pubmed/30923442 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1604197 |
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