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Molecular Therapy. Methods & Clinical Development|August 11, 2022
Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouseNicolas Wein, Tatyana A Vetter, Adeline Vulin, et al.
BMC Clinical Pathology|October 10, 2014
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image patternAna Cotta, Julia Filardi Paim, Antonio Lopes da-Cunha-Junior, et al.
Disease Models & Mechanisms|December 13, 2019
Altered <i>in vitro</i> muscle differentiation in X-linked myopathy with excessive autophagyStephanie A Fernandes, Camila F Almeida, Lucas S Souza, et al.
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