A carregar...
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...
Na minha lista:
| Main Authors: | , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|