Condition: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11


rs137852681 in CLCN2 gene and EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 PMID 19710712 2009 CLCN2 variants in idiopathic generalized epilepsy.

PMID 19191339 2009 Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.