Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome

PLoS ONE

Volumn 9, Issue 5, 2014, Pages

  Li, Xinyu ^a   Bai, Lin ^a   Fang, Jing ^a   Hou, Shengping ^a   Zhou, Qingyun ^a   Yu, Hongsong ^a   Kijlstra, Aize ^b   Yang, Peizeng ^a  

^a CHONGQING MEDICAL UNIVERSITY   (China)

^b MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 12 RECEPTOR BETA1; INTERLEUKIN 12 RECEPTOR BETA2; INTERLEUKIN 12P40; IL12B PROTEIN, HUMAN; IL12RB1 PROTEIN, HUMAN; IL12RB2 PROTEIN, HUMAN; INTERLEUKIN 12 RECEPTOR;

ADULT; ARTICLE; BEHCET DISEASE; CASE CONTROL STUDY; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAN CHINESE; HUMAN; IL 12B GENE; IL 12RBETA1 GENE; IL 12RBETA2 GENE; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; VOGT KOYANAGI SYNDROME; ALLELE; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; CLINICAL TRIAL; DNA SEQUENCE; ETHNOLOGY; GENETICS; MENINGOENCEPHALITIS;

ADULT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; BEHCET SYNDROME; CHINA; FEMALE; GENE FREQUENCY; HUMANS; INTERLEUKIN-12 SUBUNIT P40; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, INTERLEUKIN-12; SEQUENCE ANALYSIS, DNA; UVEOMENINGOENCEPHALITIC SYNDROME;

EID: 84901466489     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0098373     Document Type: Article

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