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Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in white caucasian subjects or evidence of abnormal function when expressed in vitro

Signal TransductionMolecular PhysiologyGenetic DisorderMedicineGeneticsSequence VariationsDisease Gene IdentificationWhite Caucasian SubjectsHuman Kir6.2 GeneCell BiologyCell SignalingCellular PhysiologyGene Function