Population
Homozygous weaver mice and cells expressing wvGIRK2 subunits
Design
Preclinical
Authors
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No immediate clinical implications; leaves open GIRK2 mechanisms in human channelopathies.
The weaver mutation in the GIRK2 subunit causes loss of potassium selectivity and G protein sensitivity, leading to basal nonselective channel opening and increased cell death.
Navarro et al. (1996) studied this question.
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