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1. Association between FOXP3 polymorphisms and expression and neuromyelitis optica spectrum disorder risk in the Northern Chinese Han population

Author

Liu Jing, Wang Gaoning, Yang Jiahe, Wang Yulin, Guo Ruoyi, and Li Bin

Subjects
bruton tyrosine kinase, mrna, neuromyelitis optica spectrum disorder, rs2232365, single nucleotide polymorphisms, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
Abstract

Forkhead box P3 (FOXP3) plays a critical role in the pathogenesis of autoimmune disorders. In the present study, we genotyped three single-nucleotide polymorphisms, namely, rs2232365, rs3761548, and rs3761549, to determine the relationship between FOXP3 polymorphisms and neuromyelitis optica spectrum disorder (NMOSD) susceptibility among the Northern Chinese Han population.

Published
2024
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