Mutation Screening of the γ-Aminobutyric Acid Type-A Receptor Subunit γ2 Gene in Korean Patients with Childhood Absence Epilepsy

BACKGROUND AND PURPOSE: Since the γ-aminobutyric acid type-A receptor subunit γ2 gene (GABRG2) mutation was discovered in an Australian family with childhood absence epilepsy (CAE) and febrile convulsions, a few screening studies for the GABRG2 mutation have been conducted in sporadic individuals wi...

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Detalles Bibliográficos
Autores principales: Kim, Young Ok, Kim, Myeong-Kyu, Nam, Tai-Seung, Jang, Shin Young, Park, Ki Won, Kim, Eun Young, Rho, Young Il, Woo, Young Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540286/
https://www.ncbi.nlm.nih.gov/pubmed/23323135
http://dx.doi.org/10.3988/jcn.2012.8.4.271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3540286/
https://www.ncbi.nlm.nih.gov/pubmed/23323135
http://dx.doi.org/10.3988/jcn.2012.8.4.271

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