Population
Human genes, brain and kidney tissue for mRNA localization, and Xenopus oocytes for expression studies
Design
Preclinical
Authors
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No immediate clinical implications; leaves open Kir5.1 modulation of Kir2.1 in human channelopathies.
The Kir5.1 subunit is genetically linked to Kir2.1 and functionally interacts with it to negatively regulate inward rectifying potassium channel activity.
Derst et al. (2001) studied this question.
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