KCNQ1 gain-of-function mutation in familial atrial fibrillation. [electronic resource]
Producer: 20030131Description: 251-4 p. digitalISSN:- 1095-9203
- Action Potentials
- Adolescent
- Adult
- Aged
- Animals
- Atrial Fibrillation -- genetics
- COS Cells
- Child
- China
- Chromosomes, Human, Pair 11 -- genetics
- Electrocardiography
- Female
- Haplotypes
- Heart Atria -- physiopathology
- Heart Ventricles -- physiopathology
- Humans
- KCNQ Potassium Channels
- KCNQ1 Potassium Channel
- Lod Score
- Long QT Syndrome -- genetics
- Male
- Microsatellite Repeats
- Middle Aged
- Mutation
- Mutation, Missense
- Myocytes, Cardiac -- physiology
- Patch-Clamp Techniques
- Pedigree
- Potassium Channels -- genetics
- Potassium Channels, Voltage-Gated
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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