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Weak association of a TNFRSF1A polymorphism with Behcet's disease in Chinese Han
Lili Hu
, Handan Tan
, Qingfeng Cao
, Gangxiang Yuan
, Changwei Huang
, Guannan Su
, Aize Kijlstra
, Peizeng Yang
*
*
Corresponding author for this work
MHeNs - Neuroscience
MA UECM Oogartsen MUMC
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Keyphrases
Behçet's Disease
100%
Polymorphism
100%
Han Chinese
100%
Weak Association
100%
TNFRSF1A
100%
Single nucleotide Polymorphism
40%
χ2 Test
20%
Healthy Controls
20%
Chinese Population
20%
Multiple Testing
20%
Genetic Susceptibility
20%
MassARRAY
20%
Bonferroni Correction
20%
TNF Receptor 1 (TNFR1)
20%
Fisher
20%
Chi-square
20%
Calibration Test
20%
TNFSF
20%
INIS
diseases
100%
china
100%
control
40%
nucleotides
40%
testing
20%
data
20%
patients
20%
receptors
20%
genes
20%
populations
20%
corrections
20%
genetics
20%
calibration
20%
ligands
20%
tumor necrosis factor
20%
Biochemistry, Genetics and Molecular Biology
Allele
100%
Single-Nucleotide Polymorphism
100%
TNFRSF1A
100%
Tumor Necrosis Factor Receptor
50%
Case-Control Study
50%
Genetic Susceptibility
50%
Neuroscience
Single-Nucleotide Polymorphism
100%
Tumor Necrosis Factor Receptor
50%