Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms

Pui Yan Jenny Chung, Greet Beyens, Fenna de Freitas, Steven Boonen, Piet Geusens, Filip Vanhoenacker, Leon Verbruggen, Jan Van Offel, Stefan Goemaere, Hans-Georg Zmierczak, Rene Westhovens, Jean-Pierre Devogelaer, Wim Van Hul

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)287-292
JournalMolecular Genetics and Metabolism
Volume103
Issue number3
DOIs
Publication statusPublished - Jul 2011

Keywords

  • Paget's disease of bone
  • VCP
  • RANKL
  • TNFSF11
  • IL6
  • Association

Cite this

Chung, P. Y. J., Beyens, G., de Freitas, F., Boonen, S., Geusens, P., Vanhoenacker, F., Verbruggen, L., Van Offel, J., Goemaere, S., Zmierczak, H-G., Westhovens, R., Devogelaer, J-P., & Van Hul, W. (2011). Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms. Molecular Genetics and Metabolism, 103(3), 287-292. https://doi.org/10.1016/j.ymgme.2011.03.021