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GWAS Study

Interaction between <i>G</i> <i>ALNT12</i> and <i>C1GALT1</i> Associates with Galactose-Deficient IgA1 and IgA Nephropathy.

Wang YN, Zhou XJ, Chen P et al.

33593824 PubMed ID
GWAS Study Type
1162 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WY
Wang YN
ZX
Zhou XJ
CP
Chen P
YG
Yu GZ
ZX
Zhang X
HP
Hou P
LL
Liu LJ
SS
Shi SF
LJ
Lv JC
ZH
Zhang H
Chapter II

Abstract

Summary of the research findings

Galactose-deficient IgA1 plays a key role in the pathogenesis of IgA nephropathy, the most common primary GN worldwide. Although serum levels of galactose-deficient IgA1 have a strong genetic component, the genetic link between this molecule and IgA nephropathy has not yet been clearly established.

849 Han Chinese ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

1162
Total Participants
GWAS
Study Type
Yes
Replicated
313 Han Chinese ancestry individuals
Replication Participants
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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