Persistent URL of this record https://hdl.handle.net/1887/109436
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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
- All authors
- Chung, P.Y.J.; Beyens, G.; Boonen, S.; Papapoulos, S.; Geusens, P.; Karperien, M.; Vanhoenacker, F.; Verbruggen, L.; Fransen, E.; Offel, J. van; Goemaere, S.; Zmierczak, H.G.; Westhovens, R.; Devogelaer, J.P.; Hul, W. van
- Date
- 2010-12-31
- Journal
- Human Genetics
- Volume
- 128
- Issue
- 6
- Pages
- 615 - 626