Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2

Calandra, P.; Cascino, I.; Lemmers, R.J.L.F.; Galluzzi, G.; Teveroni, E.; Monforte, M.; ... ; Deidda, G. (2016)

Article / Letter to editor

• Clinical genetics
• Diagnosis
• Molecular genetics
• Muscle disease
• Diagnostics tests

• All authors: 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; Deidda, G.
• Date: 2016-05-31
• Journal: Journal of Medical Genetics
• Volume: 53
• Issue: 5
• Pages: 348 - 355
• DOI: doi:10.1136/jmedgenet-2015-103436