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DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls.

Movement disorders : official journal of the Movement Disorder Society - 1 Jan 2004

Costa-Mallen Paola, Afsharinejad Zahra, Kelada Samir N, Costa Lucio G, Franklin Gary M, Swanson Phillip D, Longstreth W T, Viernes Hannah-Malia A, Farin Federico M, Smith-Weller Terri, Checkoway Harvey

Abstract excerpt

The allele G of the intron 13 G/A polymorphism of the monoamine oxidase B gene (MAO-B) has been associated with Parkinson's disease (PD) in several studies. Apart from a potential direct effect on splicing processes, the association of this intronic polymorphism with PD is due possibly to linkage disequilibrium with other mutations in the coding or promoter regions of the gene. We addressed this latter hypothesis...

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PMID: 14743364
DOI: 10.1002/mds.10624

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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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