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Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome
Author(s) -
Tao Zhang,
Jianping Lu,
Shaoshan Liang,
Dachen Chen,
Haitao Zhang,
Caihong Zeng,
Zhihong Liu,
Huimei Chen
Publication year - 2016
Publication title -
american journal of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 85
eISSN - 1421-9670
pISSN - 0250-8095
DOI - 10.1159/000445127
Subject(s) - atypical hemolytic uremic syndrome , factor h , missense mutation , cd46 , complement system , medicine , complement factor i , mutation , genetics , allele , population , genotype , complement factor b , immunology , gene , biology , antibody , environmental health
Genetic defects in complement proteins reportedly contribute to the atypical hemolytic uremic syndrome (aHUS). Numerous genetic studies have been published in recent years, but limited data have been gathered from Asian countries.

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