The authors have no conflict of interest to declare.
Whole-exome sequencing expands the phenotype of Hunter syndrome
Article first published online: 28 JUL 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 2, pages 172–176, August 2014
How to Cite
Nikkel, S.M., Huang, L., Lachman, R., Beaulieu, C.L., Schwartzentruber, J., FORGE Canada Consortium, Majewski, J., Geraghty, M.T. and Boycott, K.M. (2014), Whole-exome sequencing expands the phenotype of Hunter syndrome. Clinical Genetics, 86: 172–176. doi: 10.1111/cge.12236
- Issue published online: 21 JUL 2014
- Article first published online: 28 JUL 2013
- Accepted manuscript online: 11 JUL 2013 09:30AM EST
- Manuscript Accepted: 8 JUL 2013
- Manuscript Revised: 3 JUL 2013
- Manuscript Received: 31 MAY 2013
- Genome Canada
- Canadian Institutes of Health Research (CIHR)
- Ontario Genomics Institute. Grant Number: OGI-049
- Genome Québec
- Genome British Columbia
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