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A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome
Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China
A novel predictive approach for GVHD after allogeneic SCT based on clinical variables and cytokine gene polymorphisms
Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES)
Association of coding and UTR variants in the known regions with wet age-related macular degeneration in Han Chinese population
Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases
PNPLA3 rs738409 polymorphism is associated with liver fibrosis progression in patients with chronic hepatitis C: A repeated measures study
Genetic Variability in eIF2α Gene Is Associated with Islet β-Cell Function in the Development of Diabetes in a Chinese Han Population
Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population
Risk of Thrombosis in Patients Presenting with Myocardial Infarction with Nonobstructive Coronary Arteries (MINOCA)