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When Should Clinicians Order Genetic Testing for Dravet Syndrome?
The role of neuronal voltage-gated sodium channel, α-1 subunit (SCN1A) gene mutations in Dravet syndrome is well-established. With a broader phenotype than initially described, some patients lack features of Dravet syndrome as defined by the International League Against Epilepsy. We evaluated the pr...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2011
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3520060/ https://ncbi.nlm.nih.gov/pubmed/22000312 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.pediatrneurol.2011.08.001 |
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