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TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia

In inherited neurodevelopmental diseases, pathogenic processes unique to critical periods during early brain development may preclude the effectiveness of gene modification therapies applied later in life. We explored this question in a mouse model of DYT1 dystonia, a neurodevelopmental disease caus...

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Bibliografiset tiedot
Julkaisussa:J Clin Invest
Päätekijät: Li, Jay, Levin, Daniel S., Kim, Audrey J., Pappas, Samuel S., Dauer, William T.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7954593/
https://ncbi.nlm.nih.gov/pubmed/33529159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI139606
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