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Autor:
Ingrid G.M. Kolfschoten, J.C.T. van Deutekom, Anneke A.M. Janson, Suzanne Bijl, P.C. de Visser, R.E.Y. van den Eijnde, M.H.C. Zonneveld-Mulder
Publikováno v:
Neuromuscular Disorders. 23:803-804
In recent years, the field of antisense oligonucleotides (AONs) as RNA modulating therapeutics has made significant progress. Several antisense drug candidates are in (pre-) clinical development for Duchenne muscular dystrophy (DMD). Their length may