The authors have no competing financial interests or conflicts of interest to declare.
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
Version of Record online: 18 NOV 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 3, pages 220–228, September 2014
How to Cite
Filges, I., Nosova, E., Bruder, E., Tercanli, S., Townsend, K., Gibson, W.T., Röthlisberger, B., Heinimann, K., Hall, J.G., Gregory-Evans, C.Y., Wasserman, W.W., Miny, P. and Friedman, J.M. (2014), Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype. Clinical Genetics, 86: 220–228. doi: 10.1111/cge.12301
- Issue online: 20 AUG 2014
- Version of Record online: 18 NOV 2013
- Accepted manuscript online: 15 OCT 2013 11:10AM EST
- Manuscript Accepted: 11 OCT 2013
- Manuscript Revised: 29 SEP 2013
- Manuscript Received: 17 AUG 2013
- British Columbia Clinical Genomics Network (BCCGN)
- Swiss Foundation for Grants in Biology and Medicine
- Swiss National Science Foundation (SFGBM/SNSF)
- Freie Akademische Gesellschaft (FAG) Basel
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