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. Author manuscript; available in PMC: 2011 Jun 30.
Published in final edited form as: Mol Cell Endocrinol. 2010 Feb 12;322(1-2):56–63. doi: 10.1016/j.mce.2010.02.007

Figure 1.

Figure 1

Human NIS secondary structure model with all identified mutations causing iodide transport defect. For detailed characterization of mutations see table 1.

1 - 643 : amino acid residues

I – XIII : transmembrane domains