Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein

Loss of FMR1 gene function results in fragile X syndrome (FXS), the most common heritable form of intellectual disability. The protein encoded from this locus (FMRP) is an RNA binding protein thought to primarily act as a translational regulator, however recent studies implicate FMRP in other mechan...

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Detalles Bibliográficos
Autores principales: Bhogal, Balpreet, Jepson, James E., Savva, Yiannis A., Pepper, Anita S.-R., Reenan, Robert A., Jongens, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3225737/
https://www.ncbi.nlm.nih.gov/pubmed/22037499
http://dx.doi.org/10.1038/nn.2950

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3225737/
https://www.ncbi.nlm.nih.gov/pubmed/22037499
http://dx.doi.org/10.1038/nn.2950

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