| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9888280 | Clinica Chimica Acta | 2005 | 6 Pages |
Abstract
The data suggest that mutations in KCND2 and KCND3 are not a frequent cause of long QT syndrome.
Keywords
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Biochemistry, Genetics and Molecular Biology
Biochemistry
Authors
Rune Frank-Hansen, Lars Allan Larsen, Paal Andersen, Cathrine Jespersgaard, Michael Christiansen,