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GWAS Study

Whole-exome sequencing reveals the major genetic factors contributing to neuromyelitis optica spectrum disorder in Chinese patients with aquaporin 4-IgG seropositivity.

Zhong X, Chen C, Sun X et al.

33559384 PubMed ID
GWAS Study Type
1628 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZX
Zhong X
CC
Chen C
SX
Sun X
WJ
Wang J
LR
Li R
CY
Chang Y
FP
Fan P
WY
Wang Y
WY
Wu Y
PL
Peng L
LZ
Lu Z
QW
Qiu W
Chapter II

Abstract

Summary of the research findings

Background and objective: Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune disease. Although genetic factors are involved in its pathogenesis, limited evidence is available in this area. The aim of the present study was to identify the major genetic factors contributing to NMOSD in Chinese patients with aquaporin 4 (AQP4)-IgG seropositivity.

228 Chinese ancestry cases, 1,400 Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1628
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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