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  Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

Brendel, C., Belakhov, V., Werner, H., Wegener, E., Gärtner, J., Nudelman, I., et al. (2011). Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. Journal of Molecular Medicine, 89, 389-398. doi:10.1007/s00109-010-0704-4.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002A-3653-1 Version Permalink: https://hdl.handle.net/21.11116/0000-000D-3AEA-B
Genre: Journal Article

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Brendel_10.pdf (Publisher version), 768KB
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 Creators:
Brendel, Cornelia, Author
Belakhov, Valery, Author
Werner, Hauke1, Author           
Wegener, Eike, Author
Gärtner, Jutta, Author
Nudelman, Igor, Author
Baasov, Timor, Author
Huppke, Peter, Author
Affiliations:
1Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_2173664              

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Free keywords: DNA binding; Drug development; Knockout; Mutation; Molecular therapy; Pediatrics
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Language(s): eng - English
 Dates: 2011
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1007/s00109-010-0704-4
 Degree: -

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Title: Journal of Molecular Medicine
  Other : J. Mol. Med.
Source Genre: Journal
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Publ. Info: Berlin : Springer
Pages: - Volume / Issue: 89 Sequence Number: - Start / End Page: 389 - 398 Identifier: ISSN: 0946-2716
CoNE: https://pure.mpg.de/cone/journals/resource/954926989131_1