Cortical and Striatal Functional Connectivity in Juvenile-Onset Huntington’s Disease

Background: Huntington’s disease (HD) is a neurodegenerative disorder caused by a CAG repeat expansion in the HTT gene, with a rare juvenile-onset form (JoHD) marked by early, rigid motor symptoms. This study examined cortical and subcortical resting-state connectivity in JoHD, hypothesizing preserv...

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Bibliographic Details
Main Authors: Amy Barry, Peg C. Nopoulos
Format: Article
Language:English
Published: MDPI AG 2025-06-01
Series:Brain Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3425/15/6/663
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