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The First Korean Case of KCNQ2 Mutation in a Family with Benign Familial Neonatal Convulsions
Neonatal seizures represent a heterogeneous group of disorders with vastly different etiologies and outcomes. Benign familial neonatal convulsions (BFNC) are a distinctive epileptic syndrome of autosomal dominant inheritance with a favorable prognosis, characterized by the occurrence of unprovoked p...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Academy of Medical Sciences
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2811307/ https://ncbi.nlm.nih.gov/pubmed/20119593 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2010.25.2.324 |
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