CLCN2 variants in idiopathic generalized epilepsy

Nature Genetics

Volumn 41, Issue 9, 2009, Pages 954-955

  Kleefuß Lie, Ailing ^a   Friedl, Waltraut ^a   Cichon, Sven ^a   Haug, Karsten ^b   Warnstedt, Maike ^c   Alekov, Alexi ^d   Sander, Thomas ^e   Ramirez, Alfredo ^f   Poser, Barbara ^g   Maljevic, Snezana ^h   Hebeisen, Simon ⁱ   Kubisch, Christian ^f   Rebstock, Johannes ^j   Horvath, Steve ^k   Hallmann, Kerstin ^a   Dullinger, Jörn S ^l   Rau, Birgit ^a   Haverkamp, Fritz ^m   Beyenburg, Stefan ⁿ   Schulz, Herbert ^o   Janz, Dieter ^l   Giese, Bernd ^p   Müller Newen, Gerhard ^q   Propping, Peter ^a   Elger, Christian E ^a   Fahlke, Christoph ^d   Lerche, Holger ^h   more..

^a UNIVERSITY OF BONN   (Germany)

^b Ärztliche Partnerschaftsgesellschaft für Pränatal Medizin und Genetik   (Germany)

^c Pan Institut für Endokrinologie und Reproduktionsmedizin   (Germany)

^d HANNOVER MEDICAL SCHOOL   (Germany)

^e UNIVERSITY OF COLOGNE   (Germany)

^f UNIVERSITY OF COLOGNE   (Germany)

^g RWTH AACHEN UNIVERSITY   (Germany)

^h UNIVERSITY OF ULM   (Germany)

ⁱ Ionchannel Company   (Switzerland)

^j Epilepsie Zentrum Klein Wachau   (Germany)

^k UNIVERSITY OF CALIFORNIA   (United States)

^l CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^m Evangelische Fachhochschule Rheinland Westfalen Lippe   (Germany)

ⁿ CENTRE HOSPITALIER DE LUXEMBOURG   (Luxembourg)

^o MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^p UNIVERSITY OF GREIFSWALD   (Germany)

^q UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL;

AUTOSOMAL DOMINANT INHERITANCE; CLCN2 GENE; CLINICAL ARTICLE; FEMALE; GENE; GENE MUTATION; GENERALIZED EPILEPSY; GENETIC HETEROGENEITY; GRAND MAL EPILEPSY; HUMAN; LETTER; MALE; MYOCLONUS EPILEPSY; PHENOTYPE; PRIORITY JOURNAL;

CHLORIDE CHANNELS; DNA FINGERPRINTING; DNA MUTATIONAL ANALYSIS; ELECTROPHYSIOLOGY; EPILEPSY, GENERALIZED; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENETIC VARIATION; HETEROZYGOTE; HUMANS; MALE; PEDIGREE;

EID: 69349104195     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0909-954     Document Type: Letter

References (5)

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4. Blanz, J. et al. J. Neurosci. 27, 6581-6589 (2007).
5. Saint-Martin, C. et al. Hum. Mutat. 30, 397-405 (2009).