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Muscle-Specific Promoters for Gene Therapy

Many genetic diseases that are responsible for muscular disorders have been described to date. Gene replacement therapy is a state-of-the-art strategy used to treat such diseases. In this approach, the functional copy of a gene is delivered to the affected tissues using viral vectors. There is an ur...

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Detalles Bibliográficos
Autores principales: Skopenkova, V. V., Egorova, T. V., Bardina, M. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084301/
https://www.ncbi.nlm.nih.gov/pubmed/33959386
http://dx.doi.org/10.32607/actanaturae.11063