Ion-ing out the genetic variants of Kir2.1.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 35816168.
- Also identified by DOI 10.7554/eLife.80718 and PMC identifier 9273208.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Deep mutational scanning provides new insights into how mutations alter the expression and activity of the potassium ion channel Kir2.1, which is associated with many diseases.
Medical subject headings
- Potassium Channels, Inwardly Rectifying