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Article

Association of a polymorphism in intron 13 of the monoamine oxidase B gene with Parkinson disease.

American journal of medical genetics - 18 Apr 1997

Costa P, Checkoway H, Levy D, Smith-Weller T, Franklin G M, Swanson P D, Costa L G

Abstract excerpt

Monoamine oxidase B (MAO-B) is an enzyme that has relevance for Parkinson disease (PD) because of its roles in catabolizing dopamine and potentially activating exogenous neurotoxicants. A polymorphism of the gene encoding MAO-B has been identified as a single base change (A or G) in intron 13 of...

Topics

Adult
Aged
Aged, 80 and over
Alleles
Female
Genotype
Humans
Introns
Male
Middle Aged
Monoamine Oxidase
Parkinson Disease
Polymorphism, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9129714
DOI: 10.1002/(sici)1096-8628(19970418)74:2<154::aid-ajmg7>3.3.co;2-a

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9129714-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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