Persistent URL of this record https://hdl.handle.net/1887/97729
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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
- All authors
- Lemmers, R.J.L.F.; Tawil, R.; Petek, L.M.; Balog, J.; Block, G.J.; Santen, G.W.E.; Amell, A.M.; Vliet, P.J. van der; Almomani, R.; Straasheijm, K.R.; Krom, Y.D.; Klooster, R.; Sun, Y.; Dunnen, J.T. den; Helmer, Q.; Donlin-Smith, C.M.; Padberg, G.W.; Engelen, B.G.M. van; Greef, J.C. de; Aartsma-Rus, A.M.; Frants, R.R.; Visser, M. de; Desnuelle, C.; Sacconi, S.; Filippova, G.N.; Bakker, B.; Bamshad, M.J.; Tapscott, S.J.; Miller, D.G.; Maarel, S.M. van der
- Date
- 2012-12-31
- Journal
- Nature Genetics
- Volume
- 44
- Issue
- 12
- Pages
- 1370 - 1374