Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model
- Author(s):
- Greef, J.C. de (0000-0002-2819-6098); Krom, Y.D.; Hamer, B. den; Snider, L.; Hiramuki, Y.; Akker, R.F.P. van den; Breslin, K.; Pakusch, M.; Salvatori, D.C.F.; Slutter, B.; Tawil, R.; Blewitt, M.E.; Tapscott, S.J.; Maarel, S.M. van der (0000-0001-8103-711X)
- Published
- 2018
- Publication type
- Article / Letter to editor
- Date issued
- 2018-02-15
- Language
- English
- Is part of
- Human Molecular Genetics (2018), Vol. 27, no. 4, p. 716-731
- hdl
- 1887/75323
- doi
- 10.1093/hmg/ddx437
- URL
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886298/pdf/ddx437.pdf
