No competing financial interests exist. All authors declare that they do not have any conflict of interest.
National mutation study among Danish patients with hereditary haemorrhagic telangiectasia
Version of Record online: 3 OCT 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 2, pages 123–133, August 2014
How to Cite
Tørring, P.M., Brusgaard, K., Ousager, L.B., Andersen, P.E. and Kjeldsen, A.D. (2014), National mutation study among Danish patients with hereditary haemorrhagic telangiectasia. Clinical Genetics, 86: 123–133. doi: 10.1111/cge.12269
- Issue online: 21 JUL 2014
- Version of Record online: 3 OCT 2013
- Accepted manuscript online: 3 SEP 2013 12:44PM EST
- Manuscript Accepted: 29 AUG 2013
- Manuscript Revised: 23 AUG 2013
- Manuscript Received: 3 JUN 2013
- Region of Southern Denmark
|cge12269-sup-0001-TableS1.doc||Word 2007 document||30K||Table S1. Mutations in ENG, ACVRL1, and SMAD4 references [43, 56] that are previously reported [59, 60]|
Table S2. Hereditary haemorrhagic telangiectasia (HHT) families with no mutation identified.
[Correction added after first online publication on 11 October 2013: The correct Table S1 has now been uploaded.]
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