Publication | Open Access

The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes

Bone DiseaseTnfrsf11a GenesGenetic VariantsGeneticsGenetic EpidemiologyGenetic RiskOsteogenesisMedical GeneticsMedicineOsteoporosisOrthopaedic SurgeryClinical GeneticsGenetic Medicine