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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...

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Détails bibliographiques
Auteurs principaux: Lu, Jonathan T., Kass, Robert S.
Format: Artigo
Langue:Inglês
Publié: 2010
Sujets:
Accès en ligne: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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