Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations

nork Voermans, N. C., van der Bilt, R. C., IJspeert, J., Hogrel, J. Y., Jeanpierre, M., Behin, A., Laforet, P., Stojkovic, T., van Engelen, B. G., Padberg, G. W., Sacconi, S., Lemmers, R. J. L. F., van der Maarel, S. M., Eymard, B., Bassez, G.
Argitaratua izan da J Neurol (2019)

Clinical features of facioscapulohumeral muscular dystrophy 2 [Image: see text]

nork de Greef, J.C., Lemmers, R.J.L.F., Camaño, P., Day, J.W., Sacconi, S., Dunand, M., van Engelen, B.G.M., Kiuru-Enari, S., Padberg, G.W., Rosa, A.L., Desnuelle, C., Spuler, S., Tarnopolsky, M., Venance, S.L., Frants, R.R., van der Maarel, S.M., Tawil, R.
Argitaratua 2010