Lack of association between NPHS2 gene polymorphisms and Henoch-Schönlein purpura nephritis

Archives of Dermatological Research

Volumn 299, Issue 3, 2007, Pages 151-155

  Zhang, Yang ^a   Xudong, Xu ^b   Du, Lizhong ^a   Gu, Weizhong ^a   Dai, Yuwen ^a   Liu, Aimin ^a   Xia, Yonghui ^a   Mao, Jianhua ^a  

^a ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b The 117th Hospital of Chinese PLA   (China)

Author keywords

Disease susceptibility; Haplotype associations; Henoch Sch nlein Purpura nephritis; NPHS2 polymorphism

Indexed keywords

GENE PRODUCT; PODOCIN;

ADOLESCENT; ANAPHYLACTOID PURPURA; ARTICLE; CLINICAL ARTICLE; DISEASE PREDISPOSITION; DNA POLYMORPHISM; EXON; FEMALE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC PREDISPOSITION; GENOTYPE; HENOCH SCHOENLEIN PURPURA NEPHRITIS; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MALE; NEPHRITIS; NPHS2 GENE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; BIOPSY; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHINA; EXONS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; KIDNEY; MEMBRANE PROTEINS; NEPHRITIS; POLYMORPHISM, GENETIC; PURPURA, SCHOENLEIN-HENOCH;

EID: 34249703400     PISSN: 03403696     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00403-007-0752-y     Document Type: Article

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