Persistent URL of this record https://hdl.handle.net/1887/112063
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Gene variants in SMCHD1 and DNMT3B modify the risk for FSHD
- All authors
- 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
- Date
- 2016-10-31
- Journal
- Neuromuscular Disorders
- Volume
- 26
- Pages
- S152 - S152