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Human Molecular Genetics|December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophiesM Vainzof, M R Passos-Bueno, M Canovas, et al.Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.Pageof 12