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Deciphering transcription dysregulation in FSH muscular dystrophy
DUX4 , a homeobox-containing gene present in a tandem array, is implicated in facioscapulohumeral muscular dystrophy (FSHD), a dominant autosomal disease. New findings about DUX4 have raised as many fundamental questions about the molecular pathology of this unique disease as they have answered. Thi...
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| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3562129/ https://ncbi.nlm.nih.gov/pubmed/22718021 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2012.74 |
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