Gene variants in SMCHD1 and DNMT3B modify the risk for FSHD
- Author(s):
- Maarel, S. van der; Boogaard, M. van den; Lemmers, R.; Balog, J.; Mitsuhashi, S.; Kriek, M.; Wohlgemuth, M.; Kooi, E. van der; Auranen, M.; Udd, B.; Tol, M. van; Nishino, L.; Tawil, R.; Tapscott, S.; Engelen, B. van
- Published
- 2016
- Publication type
- Article / Letter to editor
- Date issued
- 2016-10-31
- Language
- English
- Is part of
- Neuromuscular Disorders (2016), Vol. 26, p. S152-S152
- hdl
- 1887/112063
- doi
- 10.1016/j.nmd.2016.06.241