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2025.02.24
Contribution of germline and somatic mutations to risk of NMOSD (Okada G, in Cell Gen.)
PRESS RELEASE
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease characterized by optic neuritis and transverse myelitis, with unclear genetic background.
A research group led by Yukinori Okada (Graduate School of Medicine, Osaka University/WPI-IFReC/The University of Tokyo/RIKEN) showed a genome-wide meta-analysis of NMOSD in Japanese (240 patients and 50,578 controls) identified significant associations with the major histocompatibility complex region and a common variant close to CCR6.
(Cell Genomics on Feb. 22, 2025)
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