None of the authors report any potential conflict of interest regarding this manuscript.
Version of Record online: 10 JAN 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 2, pages 371–376, February 2013
How to Cite
Murray, B., Wagle, R., Amat-Alarcon, N., Wilkens, A., Stephens, P., Zackai, E. H., Goldmuntz, E., Calkins, H., Deardorff, M. A. and Judge, D. P. (2013), A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome. Am. J. Med. Genet., 161: 371–376. doi: 10.1002/ajmg.a.35733
How to Cite this Article: Murray B, Wagle R, Amat-Alarcon N, Wilkens A, Stephens P, Zackai EH, Goldmuntz E, Calkins H, Deardorff MA, Judge DP. 2013. A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome. Am J Med Genet Part A 161A:371–376.
- Issue online: 24 JAN 2013
- Version of Record online: 10 JAN 2013
- Manuscript Accepted: 1 OCT 2012
- Manuscript Received: 9 APR 2012
- NIH/NICHD. Grant Number: K08HD055488
- Johns Hopkins ARVD Program
- Bogle Foundation
- Campanella family
- Wilmerding Endowment
- Dr. Francis P Chiaramonte Foundation
- Healing Hearts Foundation
- St. Jude Medical Foundation, Medtronic, Inc.
- Boston Scientific Corp
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