Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon

Premature termination of translation due to nonsense mutations is a frequent cause of inherited diseases. Therefore, many efforts were invested in the development of strategies or compounds to selectively suppress this default. Selenoproteins are interesting candidates considering the idiosyncrasy o...

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Detalles Bibliográficos
Autores principales: Rederstorff, M., Allamand, V., Guicheney, P., Gartioux, C., Richard, P., Chaigne, D., Krol, A., Lescure, A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Molecular Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248747/
https://www.ncbi.nlm.nih.gov/pubmed/18025044
http://dx.doi.org/10.1093/nar/gkm1033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248747/
https://www.ncbi.nlm.nih.gov/pubmed/18025044
http://dx.doi.org/10.1093/nar/gkm1033

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