Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1

Author(s):
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 (0000-0001-8103-711X); Horlings, C.G.C.
Published
2018
Publication type
Article / Letter to editor
disease modifiersepigeneticsfacioscapulohumeral muscular dystrophy (FSHD)genotypephenotype
Date issued
2018-12-31
Language
English
Is part of
Clinical Genetics (2018), Vol. 94, no. 6, p. 521-527
hdl
1887/86396
doi
10.1111/cge.13446