Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1

Mul, K.; Voermans, N.C.; Lemmers, R.J.L.F.; Jonker, M.A.; Vliet, P.J. van der; Padberg, G.W.; ... ; Horlings, C.G.C. (2018)

Article / Letter to editor

• disease modifiers
• epigenetics
• facioscapulohumeral muscular dystrophy (FSHD)
• genotype
• phenotype

• All authors: Mul, K.; Voermans, N.C.; Lemmers, R.J.L.F.; Jonker, M.A.; Vliet, P.J. van der; Padberg, G.W.; Engelen, B.G.M. van; Maarel, S.M. van der; Horlings, C.G.C.
• Date: 2018-12-31
• Journal: Clinical Genetics
• Volume: 94
• Issue: 6
• Pages: 521 - 527
• DOI: doi:10.1111/cge.13446