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Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy

✍ Scribed by Petra G. M. Van Overveld; Leo Enthoven; Enzo Ricci; Monica Rossi; Luciano Felicetti; Marc Jeanpierre; Sara T. Winokur; Rune R. Frants; George W. Padberg; Silvère M. Van Der Maarel

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
206 KB
Volume
58
Category
Article
ISSN
0364-5134

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Extrapolating the figures from a previous study on FSHD in a province of The Netherlands to the entire Dutch population suggests that at present a nearly complete overview is obtained of all symptomatic kindred. In 139 families, dominant inheritance was observed in 97, a pattern compatible with germ