PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome

PURPOSE: To analyze the potential association of programmed cell death 1 (PDCD1) with Vogt-Koyanagi-Harada (VKH) syndrome in a Chinese Han population. METHODS: Three single nucleotide polymorphism (SNPs), PD-1.3G/A, PD-1.5C/T, and PD-1.6G/A, were genotyped in 247 VKH patients and 289 age-, sex-, and...

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Detalles Bibliográficos
Autores principales: Meng, Qianli, Liu, Xiaoli, Yang, Peizeng, Hou, Shengping, Du, Liping, Zhou, Hongyan, Kijlstra, Aize
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2645903/
https://www.ncbi.nlm.nih.gov/pubmed/19234630

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