De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. [electronic resource]
Producer: 20060503Description: 433-40 p. digitalISSN:- 0008-6363
- Action Potentials -- physiology
- Animals
- Arrhythmias, Cardiac -- genetics
- Atrial Fibrillation -- genetics
- Computer Simulation
- DNA Mutational Analysis
- Electrocardiography
- Female
- Fetal Diseases -- genetics
- Humans
- Infant, Newborn
- KCNQ1 Potassium Channel -- genetics
- Mutation, Missense
- Oocytes
- Pregnancy
- Sinoatrial Node -- physiology
- Transfection -- methods
- Xenopus laevis
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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