Association of a PDCD1 Polymorphism With Sympathetic Ophthalmia in Han Chinese | Zendy

Jing Deng | Zendy; Jiayue Hu | Zendy; Handan Tan | Zendy; Guannan Su | Zendy; Qingfeng Cao | Zendy; Xinyue Huang | Zendy; Aize Kijlstra | Zendy; Peizeng Yang | Zendy

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Association of a PDCD1 Polymorphism With Sympathetic Ophthalmia in Han Chinese

Author(s) -

Jing Deng,

Jiayue Hu,

Handan Tan,

Guannan Su,

Qingfeng Cao,

Xinyue Huang,

Aize Kijlstra,

Peizeng Yang

Publication year - 2017

Publication title -

investigative ophthalmology and visual science

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.935

H-Index - 218

eISSN - 1552-5783

pISSN - 0146-0404

DOI - 10.1167/iovs.17-22195

Subject(s) - single nucleotide polymorphism , genotyping , genotype , vogt–koyanagi–harada disease , medicine , polymorphism (computer science) , allele , pathogenesis , genotype frequency , disease , sympathetic ophthalmia , genetics , immunology , biology , gene , uveitis

Several studies have shown that sympathetic ophthalmia (SO) and Vogt-Koyanagi-Harada (VKH) disease possess many similarities concerning their clinical manifestations. The aim of this study was to investigate whether single nucleotide polymorphisms that have been shown to be associated with VKH disease in earlier studies may also be associated with SO.

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