COMMENTED SUMMARY FROM CURRENT MEDICAL LITERATURE: HUMAN CARDIOMYOCYTES WITH LONG-QT SYNDROME IN DISH

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SEYFINEZHAD A.; BAHARVAND HOSSEIN

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Journal: ARCHIVES OF IRANIAN MEDICINE Year:2010 | Volume:13 | Issue:6 Page(s): 573-575

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Title

COMMENTED SUMMARY FROM CURRENT MEDICAL LITERATURE: HUMAN CARDIOMYOCYTES WITH LONG-QT SYNDROME IN DISH

Author(s)

SEYFINEZHAD A. | BAHARVAND HOSSEIN | Issue Writer Certificate

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Abstract

Summary: Background: Long-QT syndromes are heritable diseases associated with prolongation of the QT interval on an electrocardiogram and a high risk of sudden cardiac death due to ventricular tachyarrhythmia. In long-QT syndrome type 1, mutations occur in the KCNQ1 gene, which encodes the repolarizing potassium channel mediating the delayed rectifier I(Ks) current….

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APA: Copy

SEYFINEZHAD, A., & BAHARVAND, HOSSEIN. (2010). COMMENTED SUMMARY FROM CURRENT MEDICAL LITERATURE: HUMAN CARDIOMYOCYTES WITH LONG-QT SYNDROME IN DISH. ARCHIVES OF IRANIAN MEDICINE, 13(6), 573-575. SID. https://sid.ir/paper/280623/en

Vancouver: Copy

SEYFINEZHAD A., BAHARVAND HOSSEIN. COMMENTED SUMMARY FROM CURRENT MEDICAL LITERATURE: HUMAN CARDIOMYOCYTES WITH LONG-QT SYNDROME IN DISH. ARCHIVES OF IRANIAN MEDICINE[Internet]. 2010;13(6):573-575. Available from: https://sid.ir/paper/280623/en

IEEE: Copy

A. SEYFINEZHAD, and HOSSEIN BAHARVAND, “COMMENTED SUMMARY FROM CURRENT MEDICAL LITERATURE: HUMAN CARDIOMYOCYTES WITH LONG-QT SYNDROME IN DISH,” ARCHIVES OF IRANIAN MEDICINE, vol. 13, no. 6, pp. 573–575, 2010, [Online]. Available: https://sid.ir/paper/280623/en

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