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Article

Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.

European journal of neurology - 1 Dec 2007

Verny C, Allain P, Prudean A, Malinge M-C, Gohier B, Scherer C, Bonneau D, Dubas F, Le Gall D

Abstract excerpt

Huntington disease (HD) is a neurodegenerative disorder due to an excessive number of CAG repeats in the IT15 gene on chromosome 4. Studies of cognitive function in asymptomatic gene carriers have yielded contradictory results. This study compared cognitive performance in 44 subjects with the HD mutation (group of carriers) who had no clinical signs of HD and 39 at-risk individuals without HD mutation (group of...

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Identifiers

PMID: 17941857
DOI: 10.1111/j.1468-1331.2007.01975.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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