Showing 1 - 6 results of 6 for search 'Brockington, M', query time: 12.31s
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1
Development and spread of the Rāma narrative (pre-modern) by Brockington, J, Brockington, M
Published 2022Dataset -
2
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
Published 2001Journal article -
3
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
Published 2006Journal article -
4
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
Published 2008Journal article -
5
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
Published 2004Journal article -
6
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
Published 2007Journal article