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8. Molecular Pathogenic Basis for GABRG2 Mutations Associated With a Spectrum of Epilepsy Syndromes, From Generalized Absence Epilepsy to Dravet Syndrome. Kang JQ; Macdonald RL JAMA Neurol; 2016 Aug; 73(8):1009-16. PubMed ID: 27367160 [TBL] [Abstract][Full Text] [Related]
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