C1GALT1 polymorphisms are associated with Henoch-Schönlein purpura nephritis

Pediatric Nephrology

Volumn 27, Issue 9, 2012, Pages 1505-1509

  He, Xuelian ^a   Zhao, Peiwei ^a   Kang, Shixiu ^a   Ding, Yan ^a   Luan, Jiangwei ^a   Liu, Zhisheng ^a   Wu, Yanxiang ^a   Yin, Wei ^a  

^a Wuhan Children's Hospital   (China)

Author keywords

Aberrant galactosylation; C1GALT1; Haplotype; Henoch Sch nlein purpura nephritis; Polymorphism

Indexed keywords

ANAPHYLACTOID PURPURA; ARTICLE; C1GALT1 GENE; CASE CONTROL STUDY; CHILD; CONTROLLED STUDY; FEMALE; GENE; GENE FREQUENCY; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; HAPLOTYPE; HENOCH SCHONLEIN PURPURA NEPHRITIS; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; NEPHRITIS; PRIORITY JOURNAL; RISK; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CHILD; FEMALE; GALACTOSYLTRANSFERASES; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; NEPHRITIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PURPURA, SCHOENLEIN-HENOCH;

EID: 84864491569     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-012-2178-9     Document Type: Article

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