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Article

Study of oxidative damage and antioxidant systems in two Huntington's disease rodent models.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2013

Pérez-Severiano Francisca, Montes Sergio, Gerónimo-Olvera Cristian, Segovia José

Abstract excerpt

Huntington's disease (HD) 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. The mechanisms by which the mutation causes the disease are not completely understood yet. However, defects in the...

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Identifiers

PMID: 23754226
DOI: 10.1007/978-1-62703-411-1_12

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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