Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity

Author(s):: Sacconi, S.; Camano, P.; Greef, J.C. de (0000-0002-2819-6098); Lemmers, R.J.L.F.; Salviati, L.; Boileau, P.; Arregui, A.L.D.; Maarel, S.M. van der (0000-0001-8103-711X); Desnuelle, C.

Published: 2012
Publication type: Article / Letter to editor

Date issued: 2012-01-31
Language: English
Is part of: Journal of Medical Genetics (2012), Vol. 49, no. 1, p. 41-46
hdl: 1887/97286
doi: 10.1136/jmedgenet-2011-100101