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Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy
Mutations in the sodium channel genes SCN1A and SCN2A have been identified in monogenic childhood epilepsies, but SCN3A has not previously been investigated as a candidate gene for epilepsy. We screened a consecutive cohort of 18 children with cryptogenic partial epilepsy that was classified as phar...
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| Main Authors: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2008
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2423278/ https://ncbi.nlm.nih.gov/pubmed/18242854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2007.12.064 |
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