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Article

N-acetyltransferase polymorphism in patients with Behçet's disease.

European journal of clinical pharmacology - 1 Nov 2001

Aynacioglu A S, Bozkurt A, Nacak M, Kortunay S, Tunc R, Dincel A, Kayaalp S O

Abstract excerpt

OBJECTIVES: The objective of our study was to investigate the possible role of human arylamine N-acetyltransferase 2 (NAT2) polymorphism in susceptibility to Behçet's disease. METHODS: Eighty-five patients with Behçet's disease gave their written informed consent to participate in the study. Seven point mutations (G191A, C282T, T341C, C481T, A803G, G590A, G857A) in the NAT2 gene were analysed using polymerase...

Read the complete abstract on PubMed

Topics

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Share to Acetylation
Share to Arylamine N-Acetyltransferase
Share to Behcet Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dapsone

Share to Gene Frequency

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

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Source

Identifiers

PMID: 11791896
DOI: 10.1007/s002280100365

Genes

NAT2

Provenance

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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