Article info
Genotype-phenotype correlations
Original article
De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy
- Correspondence to Dr Erik-Jan Kamsteeg, Department of Human Genetics, Radboud University Medical Center, Nijmegen 6500 HB, The Netherlands; Erik-Jan.Kamsteeg{at}radboudumc.nl
Citation
De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy
Publication history
- Received October 7, 2014
- Revised February 1, 2015
- Accepted February 5, 2015
- First published February 27, 2015.
Online issue publication
April 16, 2015
Article Versions
- Previous version (27 February 2015).
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