The fragile X mental retardation protein has nucleic acid chaperone properties

The fragile X syndrome is the most common cause of inherited mental retardation resulting from the absence of the fragile X mental retardation protein (FMRP). FMRP contains two K-homology (KH) domains and one RGG box that are landmarks characteristic of RNA-binding proteins. In agreement with this,...

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Bibliografische gegevens
Gepubliceerd in:Nucleic Acids Res
Hoofdauteurs: Gabus, Caroline, Mazroui, Rachid, Tremblay, Sandra, Khandjian, Edouard W., Darlix, Jean-Luc
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2004
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Articles
Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC407820/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15096575/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/gkh535
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