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Article

Slow allotypic variants of the NAT2 gene and susceptibility to early-onset Parkinson's disease.

Neurology - 1 Dec 1998

Agúndez J A, Jiménez-Jiménez F J, Luengo A, Molina J A, Ortí-Pareja M, Vázquez A, Ramos F, Duarte J, Coria F, Ladero J M, Alvarez-Cermeño J C, Benítez J

Abstract excerpt

OBJECTIVE: To determine the frequency and the linkage distribution of seven mutations at the polymorphic gene coding for the arylamine N-acetyl transferase (NAT2; EC 2.3.1.5) in 121 unrelated patients with sporadic PD and in 121 unrelated healthy volunteers. METHODS: The study was performed with mutation-specific PCR using genomic DNA obtained from blood of the probands. RESULTS: Comparison of the NAT2 genotypes...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9855506
DOI: 10.1212/wnl.51.6.1587

Genes

NAT2

Provenance

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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The role of NAT2 gene polymorphism in aetiology of the most frequent neurodegenerative diseases with dementia.Semantic proximity Read ↗

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