Polymorphisms in genetics of vitamin d metabolism confer susceptibility to ocular Behçet disease in a Chinese han population

American Journal of Ophthalmology

Volumn 157, Issue 2, 2014, Pages

  Fang, Jing ^a   Hou, Shengping ^a   Xiang, Qin ^a   Qi, Jian ^a   Yu, Hongsong ^a   Shi, Yanyun ^a   Zhou, Yan ^a   Kijlstra, Aize ^b   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

VITAMIN D;

ADULT; ANKYLOSING SPONDYLITIS; ARTICLE; BEHCET DISEASE; CHINESE; CONTROLLED STUDY; CYP24A1 GENE; CYP27B1 GENE; CYP2R1 GENE; DHCR7 GENE; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; MULTIGENE FAMILY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; UVEITIS; VITAMIN D METABOLISM; VOGT KOYANAGI SYNDROME;

25-HYDROXYVITAMIN D3 1-ALPHA-HYDROXYLASE; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BEHCET SYNDROME; CASE-CONTROL STUDIES; CHINA; CHOLESTANETRIOL 26-MONOOXYGENASE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPING TECHNIQUES; HUMANS; OXIDOREDUCTASES ACTING ON CH-CH GROUP DONORS; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSPECTIVE STUDIES; STEROID HYDROXYLASES; UVEITIS, ANTERIOR; UVEOMENINGOENCEPHALITIC SYNDROME; VITAMIN D;

EID: 84892599201     PISSN: 00029394     EISSN: 18791891     Source Type: Journal    
DOI: 10.1016/j.ajo.2013.10.010     Document Type: Article

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