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Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies
Fourteen years ago, the first disease-causing mutation in a form of autosomal recessive limb-girdle muscular dystrophy was reported. Since then the number of genes has been extended to at least 14 and the phenotypic spectrum has been broadened. The generation of mouse models helped to improve our un...
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| Publicat a: | Neurotherapeutics |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer New York
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4514698/ https://ncbi.nlm.nih.gov/pubmed/19019315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nurt.2008.08.003 |
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