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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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Podrobná bibliografie
Vydáno v:J Clin Invest
Hlavní autoři: Li, Jay, Levin, Daniel S., Kim, Audrey J., Pappas, Samuel S., Dauer, William T.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Clinical Investigation 2021
Témata:
On-line přístup: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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