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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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| Publicado en: | Neurology |
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| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Lippincott Williams & Wilkins
2019
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| Materias: | |
| Acceso en línea: | 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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