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Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle
Facioscapulohumeral dystrophy (FSHD) is the third most prevalent muscular dystrophy. A progressive disease, it presents clinically as weakness and wasting of the face, shoulder and upper arm muscles, with later involvement of the trunk and lower extremities. FSHD develops through complex genetic and...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6061842/ https://ncbi.nlm.nih.gov/pubmed/29718206 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy162 |
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