Authors: Jungbluth, H Sewry, CA Brown, SC Nowak, KJ Laing, NG Wallgren-Pettersson, C Pelin, K Manzur, AY Mercuri, E Dubowitz, V Muntoni, F

Citation: H. Jungbluth et al., Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene, NEUROMUSC D, 11(1), 2001, pp. 35-40

Authors: Thirion, C Stucka, R Mendel, B Gruhler, A Jaksch, M Nowak, KJ Binz, N Laing, NG Lochmuller, H

Citation: C. Thirion et al., Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle, EUR J BIOCH, 268(12), 2001, pp. 3473-3482

Authors: Nowak, KJ Walsh, P Jacob, RL Johnsen, RD Peverall, J McNally, EM Wilton, SD Kakulas, BA Laing, NG

Citation: Kj. Nowak et al., Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion, NEUROMUSC D, 10(2), 2000, pp. 100-107

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: Mastaglia, FL Nowak, KJ Stell, R Phillips, BA Edmondston, JE Dorosz, SM Wilton, SD Hallmayer, J Kakulas, BA Laing, NG

Citation: Fl. Mastaglia et al., Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy, J NE NE PSY, 67(2), 1999, pp. 174-179