A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3
- Author(s):
- Schepers, D.; Tortora, G.; Morisaki, H.; MacCarrick, G.; Lindsay, M.; Liang, D.; Mehta, S.G.; Hague, J.; Verhagen, J.; Laar, I. van de; Wessels, M.; Detisch, Y.; Haelst, M. van; Baas, A.; Lichtenbelt, K.; Braun, K.; Linde, D. van der; Roos-Hesselink, J.; McGillivray, G.; Meester, J.; Maystadt, I.; Coucke, P.; El-Khoury, E.; Parkash, S.; Diness, B.; Risom, L.; Scurr, I.; Hilhorst-Hofstee, Y.; Morisaki, T.; Richer, J.; Desir, J.; Kempers, M.; Rideout, A.L.; Horne, G.; Bennett, C.; Rahikkala, E.; Vandeweyer, G.; Alaerts, M.; Verstraeten, A.; Dietz, H.; Laer, L. van; Loeys, B.
- Published
- 2018
- Publication type
- Article / Letter to editor
aneurysmLoeys-Dietz syndromeSMAD2SMAD3TGFB2TGFB3
- Date issued
- 2018-05-31
- Language
- English
- Is part of
- Human Mutation (2018), Vol. 39, no. 5, p. 621-634
- hdl
- 1887/86502
- doi
- 10.1002/humu.23407
- URL
- https://onlinelibrary.wiley.com/doi/epdf/10.1002/humu.23407
