SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability
- PMID: 26235738
- DOI: 10.1111/epi.13016
SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability
Comment in
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In response: SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.Epilepsia. 2015 Aug;56(8):1320. doi: 10.1111/epi.13059. Epilepsia. 2015. PMID: 26235739 No abstract available.
Comment on
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SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.Epilepsia. 2015 Mar;56(3):431-8. doi: 10.1111/epi.12925. Epub 2015 Feb 26. Epilepsia. 2015. PMID: 25785782
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