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Article

von Willebrand factor variants in C3 glomerulopathy: A Chinese cohort study.

Clinical immunology (Orlando, Fla.) - 1 Aug 2021

Chen Yun-Ying, Han Sha-Sha, Cao Yang, Yu Xiao-Juan, Zhu Li, Luo Jin-Cai, Song Wen-Chao, Yu Feng, Mao Yong-Hui, Zhao Ming-Hui

Abstract excerpt

C3 glomerulopathy (C3G) is a rare renal disease characterized by predominant glomerular C3 staining. Complement alternative pathway dysregulation due to inherited complement defects is associated with C3G. To identify novel C3G-related genes, we screened 86 genes in the complement, coagulation and endothelial systems in 35 C3G patients by targeted genomic enrichment and massively parallel sequencing....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 34245915
DOI: 10.1016/j.clim.2021.108794

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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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