Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome
- Author(s):
- Ehmke, N.; Caliebe, A.; Koenig, R.; Kant, S.G.; Stark, Z.; Cormier-Daire, V.; Wieczorek, D.; Gillessen-Kaesbach, G.; Hoff, K.; Kawalia, A.; Thiele, H.; Altmuller, J.; Fischer-Zirnsak, B.; Knaus, A.; Zhu, N.; Heinrich, V.; Huber, C.; Harabula, I.; Spielmann, M.; Horn, D.; Komak, U.; Hecht, J.; Krawitz, P.M.; Nurnberg, P.; Siebert, R.; Manzke, H.; Mundlos, S.
- Published
- 2014
- Publication type
- Article / Letter to editor
- Date issued
- 2014-12-04
- Language
- English
- Is part of
- American Journal of Human Genetics (2014), Vol. 95, no. 6, p. 763-770
- hdl
- 1887/104782
- doi
- 10.1016/j.ajhg.2014.11.004