Both authors have equally contributed to this work.
Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria†
Article first published online: 5 JUL 2012
© 2012 Wiley Periodicals, Inc.
Volume 33, Issue 10, pages 1485–1493, October 2012
How to Cite
Symoens, S., Syx, D., Malfait, F., Callewaert, B., De Backer, J., Vanakker, O., Coucke, P. and De Paepe, A. (2012), Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria. Hum. Mutat., 33: 1485–1493. doi: 10.1002/humu.22137
Communicated by Reed E. Pyeritz
- Issue published online: 13 SEP 2012
- Article first published online: 5 JUL 2012
- Accepted manuscript online: 13 JUN 2012 03:24PM EST
- Manuscript Accepted: 1 JUN 2012
- Manuscript Received: 9 MAR 2012
- Fund for Scientific Research-Flanders. Grant Number: G.0171.05
- GOA. Grant Number: 12051203
- “Geneskin” consortium of the European Commission. Grant Number: 512117
- Methusalem. Grant Number: 08/01M01108
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