Epilepsy in fragile X syndrome
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2002.tb00277.x/fullpdf
Reference25 articles.
1. FMR1 protein: conserved RNP family domains and selective RNA binding;Ashley;Science,1993
2. The course of benign partial epilepsy of childhood with centrotemporal spikes: a meta-analysis;Bouma;Neurology,1997
3. Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits;Comery;Proceedings of the National Academy of Science, USA,1997
4. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation;Devys;Nature Genetics,1993
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