De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-depent phenotyp, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.

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Maarel, S.M. van der
Deidda, G.
Lemmers, R.J.L.F.
Overveld, P.G
Wielen, M.
Hewitt, J.E.
Sandkuijl, L.A.
Bakker, B.
Ommen, G.J.B. van
Padberg, G.W.A.M. George

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