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Article

Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population.

Journal of neurology - 1 Feb 2021

Zhang Juan, Chen Mei-Jiao, Zhao Gui-Xian, Li Hong-Fu, Wu Lei, Xu Yong-Feng, Liao Yajin, Yuan Zengqiang, Wu Zhi-Ying

Abstract excerpt

BACKGROUND: The proline-rich coiled-coil 2A (PRRC2A) gene has been reported to underlie risk of various autoimmune diseases. However, no data reveal the risk susceptibility of PRRC2A to neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) so far. OBJECTIVES: To explore the association between PRRC2A variants and NMOSD and MS susceptibility in Han Chinese population. METHODS: Totally, 207...

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PMID: 32862241
DOI: 10.1007/s00415-020-10184-z

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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