Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification
Version of Record online: 21 MAY 2013
Copyright © 2013 American Society for Bone and Mineral Research
Journal of Bone and Mineral Research
Volume 28, Issue 6, pages 1378–1385, June 2013
How to Cite
Rafaelsen, S. H., Ræder, H., Fagerheim, A. K., Knappskog, P., Carpenter, T. O., Johansson, S. and Bjerknes, R. (2013), Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification. J Bone Miner Res, 28: 1378–1385. doi: 10.1002/jbmr.1850
- Issue online: 21 MAY 2013
- Version of Record online: 21 MAY 2013
- Accepted manuscript online: 16 JAN 2013 10:39AM EST
- Manuscript Accepted: 5 DEC 2012
- Manuscript Revised: 27 NOV 2012
- Manuscript Received: 24 SEP 2012
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