This work was supported in part by research grant HL-33843 and HL-51618 from the National Institutes of Health, Bethesda, MD; an unrestricted grant from BioReference Laboratory, Inc., Elmwood Park, NJ; and by the Dutch Heart Foundation 2000.059 and Foundation Leducq Transatlantic network of excellence grant (05 CVD01, preventing sudden death).
Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome
Article first published online: 13 MAR 2009
© 2009 Wiley Periodicals, Inc.
Journal of Cardiovascular Electrophysiology
Volume 20, Issue 8, pages 859–865, August 2009
How to Cite
JONS, C., MOSS, A. J., LOPES, C. M., MCNITT, S., ZAREBA, W., GOLDENBERG, I., QI, M., WILDE, A. A. M., SHIMIZU, W., KANTERS, J. K., TOWBIN, J. A., ACKERMAN, M. J. and ROBINSON, J. L. (2009), Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome. Journal of Cardiovascular Electrophysiology, 20: 859–865. doi: 10.1111/j.1540-8167.2009.01455.x
This research was carried out while Dr. Christian Jons was a Mirowski-Moss Career Development Awardee at the University of Rochester Medical Center, Rochester, NY.
Dr. Qi is a participant on ZJST 2006 Qianjiang Tellant Grant, Department of Science & Technology, Zhejiang Province, China. Dr. Shimizu is Principal Investigator on a health sciences research grant (H-18-Research on Human Genome-002) from the Ministry of Health, Labour and Welfare, Japan. Dr. Lopes reports a patent application relevant to this topic. Dr. Ackerman is a paid consultant for clinical data (formerly Genaissance Pharmaceuticals) with respect to the FAMILION genetic test for cardiac ion channel mutations.
- Issue published online: 28 JUL 2009
- Article first published online: 13 MAR 2009
- Manuscript received 2 December 2008; Revised manuscript received 12 January 2009; Accepted for publication 19 January 2009.
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