Mutations in TBL1X as a Novel Cause of Familial Central Hypothyroidism
- Author(s):
- Heinen, C.; Losekoot, M.; Sun, Y.; Watson, P.; Fairall, L.; Joustra, S.; Zwaveling-Soonawala, N.; Oostdijk, W. (0000-0003-0180-2470); Akker, E. van den; Santen, G.; Rijn, R. van; Dreschler, W.; Surovtseva, O.; Biermasz, N.; Hennekam, R.; Wit, J.; Schwabe, J.; Boelen, A.; Fliers, E.; Trotsenburg, P. van
- Published
- 2016
- Publication type
- Article / Letter to editor
- Date issued
- 2016-12-31
- Language
- English
- Is part of
- Hormone Research in Paediatrics (2016), Vol. 86, p. 55-55
- hdl
- 1887/113957