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Novel SCN1A mutation in a patient with Malignant Migrating Partial Seizures of Infancy
OBJECTIVE: A novel SCN1A mutation was discovered in a patient who clinically fulfilled the criteria for malignant migrating partial seizures of infancy. The full-term female patient had seizure onset at two months, with progression of hemiclonic, apneic, and generalized tonic-clonic seizures leading...
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| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3092158/ https://ncbi.nlm.nih.gov/pubmed/21555645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.98 |
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