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Glial progenitor cell-based treatment of the childhood leukodystrophies
The childhood leukodystrophies comprise a group of hereditary disorders characterized by the absence, malformation or destruction of myelin. These disorders share common clinical, radiological and pathological features, despite their diverse molecular and genetic etiologies. Oligodendrocytes and ast...
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| Publicado no: | Exp Neurol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5340082/ https://ncbi.nlm.nih.gov/pubmed/27170209 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2016.05.010 |
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