A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Journal of Bone and Mineral Research

• Publication date

  2012-02-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/jbmr.542PMID 21987421
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Paget disease of bone

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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

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• Genome wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget’s disease of bone

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