Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns (Q73858925)
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scientific article published on 01 June 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns |
scientific article published on 01 June 2000 |
Statements
Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns (English)
K Piippo
P Laitinen
H Swan
L Toivonen
M Viitasalo
M Pasternack
K Paavonen
H Chapman
E Hirvelä
A Sajantila