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. 2002 May 21;99(11):7774–7779. doi: 10.1073/pnas.102609499

Figure 5.

Figure 5

Coexpression with Kir2.1 mutants related to Andersen's syndrome. (A–C) In each experiment, one of the wild-type (WT) Kir2.x subunits present in guinea pig heart was coexpressed with one of the guinea pig orthologs of the mutants related to Andersen's syndrome (1). The bars represent the mean ± SEM of 11–27 experiments. (D) Three hKir2.1 mutants related to Andersen's syndrome (D71V, S136F, and R218W) were coexpressed with wild-type hKir2.1 and hKir2.3. Equal amounts of wild-type and mutant cRNA were injected in each case (n = 18–25 for each mutant).