Second-generation compound for the modulation of utrophin in the therapy of DMD

Duchenne muscular dystrophy (DMD) is a lethal, X-linked muscle-wasting disease caused by lack of the cytoskeletal protein dystrophin. There is currently no cure for DMD although various promising approaches are progressing through human clinical trials. By pharmacologically modulating the expression...

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Bibliografski detalji
Glavni autori: Guiraud, S, Squire, S, Edwards, B, Chen, H, Burns, D, Shah, N, Babbs, A, Davies, S, Wynne, G, Russell, A, Elsey, D, Wilson, F, Tinsley, J, Davies, K
Format: Journal article
Jezik:English
Izdano: Oxford University Press 2015