Potassium Channel Subunits: The MiRP Family

  Figure 7.
Figure 7.

Schematic of the MiRP2 peptide indicating a mutation associated with familial periodic paralysis. The residue highlighted in red represents a missense mutation (i.e., R83H) that is associated with disease (CHO, predicted sites of glycosylation; P, predicted sites of phosphorylation).

This Article

  1. MI June 2001 vol. 1 no. 2 95-107