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Article

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

Molecular vision - 3 Jun 2009

Horie Yukihiro, Kitaichi Nobuyoshi, Katsuyama Yoshihiko, Yoshida Kazuhiko, Miura Toshie, Ota Masao, Asukata Yuri, Inoko Hidetoshi, Mizuki Nobuhisa, Ishida Susumu, Ohno Shigeaki

Abstract excerpt

PURPOSE: Vogt-Koyanagi-Harada (VKH) disease is an autoimmune disorder against melanocytes. Polymorphisms of the protein tyrosine phosphatase non-receptor 22 gene (PTPN22) have recently been reported to be associated with susceptibility to several autoimmune diseases. In this study, genetic susceptibility to VKH disease was investigated by screening for single nucleotide polymorphisms (SNPs) of PTPN22. METHODS: A...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Linkage Disequilibrium

Share to Polymorphism, Single Nucleotide

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 22

Share to Sequence Analysis, DNA

Share to Uveomeningoencephalitic Syndrome

Source

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Identifiers

PMID: 19503742
PMCID: PMC2690962

Genes

PTPN22

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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