We read with great interest the article by Torisu et al. who reported “Girl with a
PRRT2 mutation and infantile focal epilepsy with bilateral spikes” [
[1]
].- Torisu H.
- Watanabe K.
- Shimojima K.
- Sugawara M.
- Sanefuji M.
- Ishizaki Y.
- et al.
Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes.
Brain Dev. 2013; https://doi.org/10.1016/j.braindev.2013.05.009
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References
- Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes.Brain Dev. 2013; https://doi.org/10.1016/j.braindev.2013.05.009
- Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.Brain. 2011; 134: 3493-3501
- Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis.J Med Genet. 2012; 49: 76-78
- Mild paroxysmal kinesigenic dyskinesia caused by PRRT2 missense mutation with reduced penetrance.Neurology. 2012; 79: 46-48
Article info
Publication history
Published online: September 26, 2013
Accepted:
September 6,
2013
Received in revised form:
September 5,
2013
Received:
June 5,
2013
Identification
Copyright
© 2013 The Japanese Society of Child Neurology. Published by Elsevier Inc. All rights reserved.
