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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Detalles Bibliográficos
Autores principales: Yum, Mi-Sun, Ko, Tae-Sung, Yoo, Han-Wook
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811307/
https://www.ncbi.nlm.nih.gov/pubmed/20119593
http://dx.doi.org/10.3346/jkms.2010.25.2.324

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811307/
https://www.ncbi.nlm.nih.gov/pubmed/20119593
http://dx.doi.org/10.3346/jkms.2010.25.2.324

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