Yilmaz, HurriyetZateri, CoskunUludağ, AhmetBakar, CoskunKosar, SuleÖzdemir, Öztürk2025-01-272025-01-2720120736-02661554-527Xhttps://doi.org/10.1002/jor.22075https://hdl.handle.net/20.500.12428/27621The role of genetics in the etiopathogenesis of adolescent idiopathic scoliosis (AIS) is unclear. In this study, we investigated the relationship between AIS and polymorphisms in MATN-1, LCT C/T-13910, and VDR BsmI genes. 53 Turkish adolescents with diagnosed AIS and 54 healthy adult individuals were included in the study. MATN-1, LCT C/T-13910, and VDR BsmI gene mutations were analyzed with real-time PCR. We did not detect a statistically significant difference between AIS and control groups in respect to those three different gene polymorphisms (p?eninfo:eu-repo/semantics/closedAccessadolescent idiopathic scoliosiscurve progressionlactose gene polymorphismmatrilin gene polymorphismvitamin d receptor gene polymorphismArticle3091459146310.1002/jor.22075Q1WOS:0003063114000162-s2.0-8486385423722278929Q1