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Association between FOXP3 polymorphisms and expression and neuromyelitis optica spectrum disorder risk in the Northern Chinese Han population
- Source :
- Translational Neuroscience, Vol 15, Iss 1, Pp 1450-61 (2024)
- Publication Year :
- 2024
- Publisher :
- De Gruyter, 2024.
-
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.
Details
- Language :
- English
- ISSN :
- 20816936
- Volume :
- 15
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Translational Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.b2b9627280d84ad6b8af1491ac60ebc8
- Document Type :
- article
- Full Text :
- https://doi.org/10.1515/tnsci-2022-0337