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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Vydáno v:Neurology
Hlavní autoři: Tereshchenko, Alexander, Magnotta, Vincent, Epping, Eric, Mathews, Katherine, Espe-Pfeifer, Patricia, Martin, Erin, Dawson, Jeffrey, Duan, Wenzhen, Nopoulos, Peg
Médium: Artigo
Jazyk:Inglês
Vydáno: Lippincott Williams & Wilkins 2019
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Article
On-line přístup: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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