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Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population
LINE-1 hypomethylation is associated to specific clinico-pathological features in Stage I non-small cell lung cancer
A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats
Correlations between BDNF genetic polymorphism and postpartum depression in cesarean section parturient
Differences in ABCA1 R219K polymorphisms and serum indexes in Alzheimer and Parkinson Diseases in Northern China
Association between regulator of telomere elongation helicase1 (RTEL1) gene and HAPE risk: A case-control study
Genetic and clinical determinants of mizoribine pharmacokinetics in renal transplant recipients
Genetics and Age-Related Eye Disease Study Formulation Interaction in Neovascular Age-Related Macular Degeneration
Correlation analysis between CARMEN variants and alcohol-induced osteonecrosis of the femoral head in the Chinese population
A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1
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