Large deletions of the KCNH2 (HERG) gene: a novel genetic mechanism for the Long QT syndrome type 2
| Autor: | Vincent Probst, Schmitt, S., Briec, F., Barc, J., Le Cunff, M., Vieyres, C., Le Caignec, C., Kyndt, F., Le Marec, H., Schott, J. J. |
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| Zdroj: | ResearcherID |
| Databáze: | OpenAIRE |
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