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Citation: K. Oexle et A. Kohlschutter, Cause of progression in Duchenne muscular dystrophy: Impaired differentiation more probable than replicative aging, NEUROPEDIAT, 32(3), 2001, pp. 123-129

Authors: Gong, YQ Slee, RB Fukai, N Rawadi, G Roman-Roman, S Reginato, AM Wang, HW Cundy, T Glorieux, FH Lev, D Zacharin, M Oexle, K Marcelino, J Suwairi, W Heeger, S Sabatakos, G Apte, S Adkins, WN Allgrove, J Arslan-Kirchner, M Batch, JA Beighton, P Black, GCM Boles, RG Boon, LM Borrone, C Brunner, HG Carle, GF Dallapiccola, B De Paepe, A Floege, B Halfhide, ML Hall, B Hennekam, RC Hirose, T Jans, A Juppner, H Kim, CA Keppler-Noreuil, K Kohlschuetter, A LaCombe, D Lambert, M Lemyre, E Letteboer, T Peltonen, L Ramesar, RS Romanengo, M Somer, H Steichen-Gersdorf, E Steinmann, B Sullivan, B Superti-Furga, A Swoboda, W van den Boogaard, MJ Van Hul, V Vikkula, M Votruba, M Zabel, B Garcia, T Baron, R Olsen, BR Warman, ML

Citation: Yq. Gong et al., LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development, CELL, 107(4), 2001, pp. 513-523

Authors: Young, P Stogbauer, F Eller, B de Jonghe, P Lofgren, A Timmerman, V Rautenstrauss, B Oexle, K Grehl, H Kuhlenbaumer, G Van Broeckhoven, C Ringelstein, EB Funke, H

Citation: P. Young et al., PMP22 Thr118Met is not a clinically relevant CMT1 marker, J NEUROL, 247(9), 2000, pp. 696-700

Authors: Nowak, KJ Wattanasirichaigoon, D Goebel, HH Wilce, M Pelin, K Donner, K Jacob, RL Hubner, C Oexle, K Anderson, JR Verity, CM North, KN Iannaccone, ST Muller, CR Nurnberg, P Muntoni, F Sewry, C Hughes, I Sutphen, R Lacson, AG Swoboda, KJ Vigneron, J Wallgren-Pettersson, C Beggs, AH Laing, NG

Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212

Authors: Oexle, K Heyer, R

Citation: K. Oexle et R. Heyer, On dystrophin abundance and C-terminal missense mutations in dystrophinopathies, ANN NEUROL, 46(1), 1999, pp. 137-138