Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome

Author(s):
Lemmers, R.J.L.F.; Boogaard, M.L. van den; Vliet, P.J. van der; Donlin-Smith, C.M.; Nations, S.P.; Ruivenkamp, C.A.L.; Heard, P.; Bakker, B.; Tapscott, S.; Cody, J.D.; Tawil, R.; Maarel, S.M. van der (0000-0001-8103-711X)
Published
2015
Publication type
Article / Letter to editor
FSHDSMCHD1epigenetic modifierD4Z4epiallele
Date issued
2015-07-31
Language
English
Is part of
Human Mutation (2015), Vol. 36, no. 7, p. 679-683
hdl
1887/100926
doi
10.1002/humu.22792