A family of delayed rectifier voltage-gated potassium channels that share homology with their founding member, KCNQ1 PROTEIN. KCNQ potassium channels have been implicated in a variety of diseases including LONG QT SYNDROME; DEAFNESS; and EPILEPSY.
Subtype terms (3)
More specific conditions that are subtypes of KCNQ Potassium Channels in the MeSH hierarchy.