Genetic variant of WIF1 gene is functionally associated with developmental dysplasia of the hip in Han Chinese population.

ABSTRACT: Developmental dysplasia of the hip (DDH) is a common skeletal disorder. Studies have demonstrated a significant role of WIF1 gene in skeletal development. The present study was conducted to reveal the association between DDH and gene WIF1. A two-stage case-control candidate gene association study was conducted in total 1573 samples (586 DDH patients and 987 healthy controls) in this study. Polymorphism rs3782499 was genotyped in all samples. Difference of WIF1 expression in hip joint tissue was compared between the patients and the controls. WIF1 expression was compared among different genotypes in DDH patients. The SNP rs3782499 was found significantly associated with DDH in the two-stage study with 585 patients and 987 controls. There was a significant difference in allele frequency (p =

SUBMITTER: Sun Y 

PROVIDER: S-EPMC6342943 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature