LEMMERS , Richard J.l.f.

Objective To compare the clinical features of patients showing a classical phenotype of facioscapulohumeral muscular dystrophy (FSHD) with genetic and epigenetic characteristics of the FSHD1 and FSHD2 loci D4Z4 and SMCHD1.Methods This is a national multicenter cohort study. We measured motor strength, motor function, and disease severity by...