Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2

Author(s):: Calandra, P.; Cascino, I.; Lemmers, R.J.L.F.; Galluzzi, G.; Teveroni, E.; Monforte, M.; Tasca, G.; Ricci, E.; Moretti, F.; Maarel, S.M. van der (0000-0001-8103-711X); Deidda, G.

Published: 2016
Publication type: Article / Letter to editor

Clinical geneticsDiagnosisMolecular geneticsMuscle diseaseDiagnostics tests

Date issued: 2016-05-31
Language: English
Is part of: Journal of Medical Genetics (2016), Vol. 53, no. 5, p. 348-355
hdl: 1887/113795
doi: 10.1136/jmedgenet-2015-103436