None to declare.
Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT
Article first published online: 5 JUN 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 4, pages 359–364, April 2014
How to Cite
Davis, E.E., Savage, J.H., Willer, J.R., Jiang, Y.-H., Angrist, M., Androutsopoulos, A. and Katsanis, N. (2014), Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT. Clinical Genetics, 85: 359–364. doi: 10.1111/cge.12189
- Issue published online: 10 MAR 2014
- Article first published online: 5 JUN 2013
- Accepted manuscript online: 8 MAY 2013 12:36PM EST
- Manuscript Revised: 6 MAY 2013
- Manuscript Accepted: 6 MAY 2013
- Manuscript Received: 29 DEC 2012
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