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Brain structure in juvenile-onset Huntington disease
OBJECTIVE: To assess brain morphometry in a sample of patients with juvenile-onset Huntington disease (JOHD) and several mouse models of Huntington disease (HD) that likely represent the human JOHD phenotype. METHODS: Despite sharing the mutation in the Huntingtin gene, adult-onset HD characteristic...
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| Pubblicato in: | Neurology |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Lippincott Williams & Wilkins
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6511077/ https://ncbi.nlm.nih.gov/pubmed/30971481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000007355 |
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