No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy

Nature Genetics

Volumn 42, Issue 1, 2010, Pages 3-

  Niemeyer, María I ^a   Cid, L Pablo ^a   Seplveda, Francisco V ^a   Blanz, Judith ^b   Auberson, Muriel ^c   Jentsch, Thomas J ^d  

^a CENTRO DE ESTUDIOS CIENTÍFICOS CECS   (Chile)

^b UNIVERSITY OF KIEL   (Germany)

^c UNIVERSITY OF LAUSANNE   (Switzerland)

^d LEIBNIZ INSTITUT FÜR MOLEKULARE PHARMAKOLOGIE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

AMINO ACID SUBSTITUTION; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENERALIZED EPILEPSY; GENETIC VARIABILITY; GENOTYPE; IDIOPATHIC GENERALIZED EPILEPSY; LETTER; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RNA SPLICING;

CHLORIDE CHANNELS; EPILEPSY, GENERALIZED; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HETEROZYGOTE; HUMANS; MUTATION;

EID: 73349099352     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0110-3     Document Type: Letter

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