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Recent progress in congenital long QT syndrome
PURPOSE OF REVIEW: As genetic testing for long QT syndrome (LQTS) has become readily available, important advances are being made in understanding the exact link between ion channel mutation and observed phenotype. This paper reviews recent findings in the literature. RECENT FINDINGS: Congenital LQT...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2010
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3151313/ https://ncbi.nlm.nih.gov/pubmed/20224391 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/HCO.0b013e32833846b3 |
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