Long QT syndrome: from genetic basis to treatment
The congenital long QT syndrome (LQTS) is a monogenic disorder, not as rare as it was originally estimated to be, mainly caused by mutations in genes encoding for ion channels. Molecular screening in this disease is part of the diagnostic process and this has already been recognized by current guide...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI AG
2011-12-01
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| Col·lecció: | Cardiogenetics |
| Matèries: | |
| Accés en línia: | http://www.pagepressjournals.org/index.php/cardiogen/article/view/241 |
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