A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents. [electronic resource]
Producer: 20120917Description: 666-73 p. digitalISSN:- 1755-3245
- Action Potentials -- physiology
- Animals
- Cells, Cultured
- Child
- Electrocardiography
- Female
- Genetic Predisposition to Disease -- genetics
- HEK293 Cells
- Heterozygote
- Homozygote
- Humans
- Lown-Ganong-Levine Syndrome -- genetics
- Models, Animal
- Mutation -- genetics
- Myocytes, Cardiac -- cytology
- Patch-Clamp Techniques
- Pedigree
- Potassium Channels, Inwardly Rectifying -- genetics
- Rats
- Rats, Wistar
- Transfection
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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