Reducing huntingtin by immunotherapy delays disease progression in a mouse model of Huntington disease
In Huntington disease (HD), the mutant huntingtin (mtHTT) protein is the principal cause of pathological changes that initiate primarily along the cortico-striatal axis. mtHTT is ubiquitously expressed and there is, accordingly, growing recognition that HD is a systemic disorder with functional inte...
| Published in: | Neurobiology of Disease |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-01-01
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| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996123003923 |
