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Clinical and genetic characteristics of late‐onset Huntington's disease in a large European cohort

BACKGROUND AND PURPOSE: Huntington's disease (HD) is an autosomal dominant condition caused by CAG‐triplet repeat expansions. CAG‐triplet repeat expansion is inversely correlated with age of onset in HD and largely determines the clinical features. The aim of this study was to examine the pheno...

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Detalles Bibliográficos
Autores principales:	Petracca, Martina, Di Tella, Sonia, Solito, Marcella, Zinzi, Paola, Lo Monaco, Maria Rita, Di Lazzaro, Giulia, Calabresi, Paolo, Silveri, Maria Caterina, Bentivoglio, Anna Rita
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Movement Disorders
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324106/ https://www.ncbi.nlm.nih.gov/pubmed/35357736 http://dx.doi.org/10.1111/ene.15340

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