SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity
Article first published online: 17 APR 2013
Copyright © 2013 American Society for Bone and Mineral Research
Journal of Bone and Mineral Research
Volume 28, Issue 5, pages 1041–1049, May 2013
How to Cite
Pangrazio, A., Fasth, A., Sbardellati, A., Orchard, P. J., Kasow, K. A., Raza, J., Albayrak, C., Albayrak, D., Vanakker, O. M., De Moerloose, B., Vellodi, A., Notarangelo, L. D., Schlack, C., Strauss, G., Kühl, J.-S., Caldana, E., Lo Iacono, N., Susani, L., Kornak, U., Schulz, A., Vezzoni, P., Villa, A. and Sobacchi, C. (2013), SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. J Bone Miner Res, 28: 1041–1049. doi: 10.1002/jbmr.1849
- Issue published online: 17 APR 2013
- Article first published online: 17 APR 2013
- Accepted manuscript online: 21 DEC 2012 10:57AM EST
- Manuscript Accepted: 5 DEC 2012
- Manuscript Revised: 21 NOV 2012
- Manuscript Received: 9 OCT 2012
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