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Canavan Disease as a Model for Gene Therapy-Mediated Myelin Repair
In recent years, the scientific and therapeutic fields for rare, genetic central nervous system (CNS) diseases such as leukodystrophies, or white matter disorders, have expanded significantly in part due to technological advancements in cellular and clinical screenings as well as remedial therapies...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102781/ https://www.ncbi.nlm.nih.gov/pubmed/33967698 http://dx.doi.org/10.3389/fncel.2021.661928 |