Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

CLCN2 variants in idiopathic generalized epilepsy

Item Type:Letter
Title:CLCN2 variants in idiopathic generalized epilepsy
Creators Name:Kleefuss-Lie, A. and Friedl, W. and Cichon, S. and Haug, K. and Warnstedt, M. and Alekov, A. and Sander, T. and Ramirez, A. and Poser, B. and Maljevic, S. and Hebeisen, S. and Kubisch, C. and Rebstock, J. and Horvath, S. and Hallmann, K. and Dullinger, J.S. and Rau, B. and Haverkamp, F. and Beyenburg, S. and Schulz, H. and Janz, D. and Giese, B. and Muller-Newen, G. and Propping, P. and Elger, C.E. and 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 (U.S.A.)
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

Repository Staff Only: item control page

Open Access
MDC Library