These authors contributed equally to this work.
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome—Osteogenesis imperfecta phenotypic spectrum†
Article first published online: 5 JUL 2012
© 2012 Wiley Periodicals, Inc.
Volume 33, Issue 10, pages 1444–1449, October 2012
How to Cite
Puig-Hervás, M. T., Temtamy, S., Aglan, M., Valencia, M., Martínez-Glez, V., Ballesta-Martínez, M. J., López-González, V., Ashour, A. M., Amr, K., Pulido, V., Guillén-Navarro, E., Lapunzina, P., Caparrós-Martín, J. A. and Ruiz-Perez, V. L. (2012), Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome—Osteogenesis imperfecta phenotypic spectrum. Hum. Mutat., 33: 1444–1449. doi: 10.1002/humu.22133
Communicated by Raymond Dalgleish
- Issue published online: 13 SEP 2012
- Article first published online: 5 JUL 2012
- Accepted manuscript online: 11 JUN 2012 10:21AM EST
- Manuscript Accepted: 23 MAY 2012
- Manuscript Received: 23 FEB 2012
- The Spanish Ministry of Science and Innovation. Grant Number: SAF2010-17901
- The Centro de Investigación Biomédica en Red de Enfermedades Raras Programa de Investigación de Enfermedades Pediátricas
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