These authors contributed equally to this work.
Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness
Article first published online: 11 SEP 2012
© 2012 John Wiley & Sons A/S
Volume 83, Issue 5, pages 457–461, May 2013
How to Cite
Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness., , , , , , , , , , .
J. R. L. is a consultant for Athena Diagnostics, has stock ownership in 23andMe and Ion Torrent Systems, and is a co-inventor on multiple United States and European patents for DNA diagnostics. R. A. G. was a founding shareholder in Seq-Wright, Inc. Some of the authors are based in the Department of Molecular and Human Genetics at Baylor College of Medicine, which derives revenue from genetic laboratory testing, including whole-exome sequencing. The remaining authors have no conflicts of interest to declare.
- Issue published online: 5 APR 2013
- Article first published online: 11 SEP 2012
- Accepted manuscript online: 17 AUG 2012 10:36AM EST
- Manuscript Accepted: 7 AUG 2012
- Manuscript Revised: 3 AUG 2012
- Manuscript Received: 11 JUL 2012
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