Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A. (Q33149057)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A. |
scientific article |
Statements
Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A (English)
Aimée Paulussen
Gert Matthijs
Peter Verhasselt
Nadine Cohen
Jeroen Aerssens
1 January 2003