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Article

Oxidative damage in Huntington's disease.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2004

Segovia José, Pérez-Severiano Francisca

Abstract excerpt

Huntington's disease is a hereditary neurodegenerative disorder, characterized by motor, psychiatric, and cognitive symptoms. The genetic defect responsible for the onset of the disease, expansion of CAG repeats in exon 1 of the gene that codes for huntingtin, has been unambiguously identified. On the other hand, the mechanisms by which the mutation causes the disease are not completely understood yet. However,...

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PMID: 15201466
DOI: 10.1385/1-59259-804-8:321

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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