Clinical and genetic analysis of familial neuromyelitis optica spectrum disorder in Chinese: associated with ubiquitin-specific peptidase USP18 gene variants.
Yanyu ChangLuyao ZhouXiaonan ZhongZiyan ShiXiaobo SunYuge WangRui LiYou-Ming LongHongyu ZhouChao QuanAllan G KermodeQingfen YuWei QiuPublished in: Journal of neurology, neurosurgery, and psychiatry (2022)
with impaired intronic regulatory function contributed to the pathogenesis of NMOSD.