Lack of association of miR-146a and Ets-1 gene polymorphisms with Fuchs uveitis syndrome in Chinese Han patients

Molecular Vision

Volumn 18, Issue , 2012, Pages 426-430

  Zhou, Qingyun ^a   Kijlstra, Aize ^b   Hou, Shengping ^a   Yu, Hongsong ^a   Zhang, Xuedong ^a   Li, Xinyu ^a   Xiao, Xiang ^a   Yang, Peizeng ^a  

^a THE FIRST AFFILIATED HOSPITAL OF CHONGQING MEDICAL UNIVERSITY   (China)

^b MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHINESE; CONTROLLED STUDY; ETS 1 GENE; FEMALE; FUCHS UVEITIS SYNDROME; GENE FREQUENCY; GENE FUNCTION; GENE PRODUCT; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MIR 146A GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; UVEITIS;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHINA; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; HUMANS; MALE; MICRORNAS; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEIN C-ETS-1; SYNDROME; UVEITIS, ANTERIOR; YOUNG ADULT;

EID: 84863280327     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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