Development and spread of the Rāma narrative (pre-modern) by Brockington, J, Brockington, M

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dyst... by Brockington, M, Blake, D, Prandini, P, Brown, S, Torelli, S, Benson, M, Ponting, C, Estournet, B, Romero, N, Mercuri, E, Voit, T, Sewry, C, Guicheney, P, Muntoni, F

gene mutations in steroid-responsive limb girdle muscular dystrophy by Godfrey, C, Escolar, D, Brockington, M, Clement, E, Mein, R, Jimenez-Mallebrera, C, Torelli, S, Feng, L, Brown, S, Sewry, C, Rutherford, M, Shapira, Y, Abbs, S, Muntoni, F

Mild POMGnT1 Mutations Underlie a Novel Limb-Girdle Muscular Dystrophy Variant by Clement, E, Godfrey, C, Tan, J, Brockington, M, Torelli, S, Feng, L, Brown, S, Jimenez-Mallebrera, C, Sewry, C, Longman, C, Mein, R, Abbs, S, Vajsar, J, Schachter, H, Muntoni, F

Congenital muscular dystrophy with short stature, proximal contractures and distal laxity. by Mercuri, E, Lampe, A, Straub, V, Yuva, Y, Longman, C, Wright, M, Brown, S, Sewry, C, Bonnemann, C, Kinali, M, Brockington, M, Hausser, I, Hilton Jones, D, Voit, T, Bushby, K, Muntoni, F

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan by Godfrey, C, Clement, E, Mein, R, Brockington, M, Smith, J, Talim, B, Straub, V, Robb, S, Quinlivan, R, Feng, L, Jimenez-Mallebrera, C, Mercuri, E, Manzur, A, Kinali, M, Torelli, S, Brown, S, Sewry, C, Bushby, K, Topaloglu, H, North, K, Abbs, S, Muntoni, F