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Abnormal development of cerebellar-striatal circuitry in Huntington disease
OBJECTIVE: To test the hypothesis that the trajectory of functional connections over time of the striatum and the cerebellum differs between presymptomatic patients with the Huntington disease (HD) gene expansion (GE) and patients with a family history of HD but without the GE (GNE), we evaluated fu...
Tallennettuna:
| Julkaisussa: | Neurology |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Lippincott Williams & Wilkins
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7274924/ https://ncbi.nlm.nih.gov/pubmed/32265233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000009364 |
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