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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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| Udgivet i: | Exp Neurol |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2016
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| Fag: | |
| Online adgang: | 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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