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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 3, 2023. (Total: 223614Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Long QT Syndrome and SNTA1[original query]
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.
Circulation. Arrhythmia and electrophysiology 2008 Aug 1 (3): 193-201.
Wu Geru, Ai Tomohiko, Kim Jeffrey J, Mohapatra Bhagyalaxmi, Xi Yutao, Li Zhaohui, Abbasi Shahrzad, Purevjav Enkhsaikhan, Samani Kaveh, Ackerman Michael J, Qi Ming, Moss Arthur J, Shimizu Wataru, Towbin Jeffrey A, Cheng Jie, Vatta Matt
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.
Circulation. Arrhythmia and electrophysiology 2009 Dec 2 (6): 667-76.
Cheng Jianding, Van Norstrand David W, Medeiros-Domingo Argelia, Valdivia Carmen, Tan Bi-hua, Ye Bin, Kroboth Stacie, Vatta Matteo, Tester David J, January Craig T, Makielski Jonathan C, Ackerman Michael
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
Journal of the American College of Cardiology 2010 12 57 (1): 40-7.
Barc Julien, Briec François, Schmitt Sébastien, Kyndt Florence, Le Cunff Martine, Baron Estelle, Vieyres Claude, Sacher Frédéric, Redon Richard, Le Caignec Cédric, Le Marec Hervé, Probst Vincent, Schott Jean-Jacqu
Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61.
Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy
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