CLCN2 variants in idiopathic generalized epilepsy

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Item Type:	Letter
Title:	CLCN2 variants in idiopathic generalized epilepsy
Creators Name:	Kleefuss-Lie, A., Friedl, W., Cichon, S., Haug, K., Warnstedt, M., Alekov, A., Sander, T., Ramirez, A., Poser, B., Maljevic, S., Hebeisen, S., Kubisch, C., Rebstock, J., Horvath, S., Hallmann, K., Dullinger, J.S., Rau, B., Haverkamp, F., Beyenburg, S., Schulz, H., Janz, D., Giese, B., Muller-Newen, G., Propping, P., Elger, C.E., Fahlke, C. and Lerche, H.
Keywords:	Chloride Channels, DNA Fingerprinting, DNA Mutational Analysis, Electrophysiology, Generalized Epilepsy, Family Health, Dominant Genes, Genetic Predisposition to Disease, Genetic Screening, Genetic Variation, Heterozygote, Pedigree
Source:	Nature Genetics
ISSN:	1061-4036
Publisher:	Nature Publishing Group
Volume:	41
Number:	9
Page Range:	954-955
Date:	September 2009
Official Publication:	https://doi.org/10.1038/ng0909-954
PubMed:	View item in PubMed

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