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New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile convulsions) families

Allelic VariantDevelopmental BiologyMolecular PhysiologyCotransporter GeneInfantile ConvulsionsGeneticsPhysiologyGenetic DisorderHuman PolymorphismMolecular GeneticsMedical GeneticsMutation AnalysisDisease Gene IdentificationMedicineClinical Genetics