How to Cite this Article: van Steensel MAM, Oranje AP, van der Schroeff JG, Wagner A, van Geel M. 2009. The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. Am J Med Genet Part A 149A:657–661.
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron†
Article first published online: 16 MAR 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 4, pages 657–661, April 2009
How to Cite
van Steensel, M.A.M., Oranje, A.P., van der Schroeff, J.G., Wagner, A. and van Geel, M. (2009), The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. Am. J. Med. Genet., 149A: 657–661. doi: 10.1002/ajmg.a.32744
- Issue published online: 24 MAR 2009
- Article first published online: 16 MAR 2009
- Manuscript Accepted: 30 DEC 2008
- Manuscript Received: 12 AUG 2008
- ZON-MW Clinical Fellowship. Grant Number: 907-00-202
- Foundation for Ichthyosis and Related Skin Types (F.I.R.S.T.)
- Maastricht University Medical Center
- GROW Research Institute for Oncology and Developmental Biology
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