Autosomal Dominant Inheritance of Centrotemporal Sharp Waves in Rolandic Epilepsy Families

PURPOSE: Centrotemporal sharp (CTS) waves, the electroencephalogram (EEG) hallmark of rolandic epilepsy, are found in approximately 4% of the childhood population. The inheritance of CTS is presumed autosomal dominant but this is controversial. Previous studies have varied considerably in methodolog...

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Huvudupphovsmän: Bali, Bhavna, Kull, Lewis L., Strug, Lisa J., Clarke, Tara, Murphy, Peregrine L., Akman, Cigdem I., Greenberg, David A., Pal, Deb K.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2007
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2150739/
https://ncbi.nlm.nih.gov/pubmed/17662063
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1528-1167.2007.01221.x
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