These authors contributed equally to this work.
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes
Version of Record online: 17 SEP 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 86, Issue 2, pages 142–148, August 2014
How to Cite
Weh, E., Reis, L.M., Tyler, R.C., Bick, D., Rhead, W.J., Wallace, S., McGregor, T.L., Dills, S.K., Chao, M.-C., Murray, J.C. and Semina, E.V. (2014), Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical Genetics, 86: 142–148. doi: 10.1111/cge.12241
The authors declare no conflict of interest.
- Issue online: 21 JUL 2014
- Version of Record online: 17 SEP 2013
- Accepted manuscript online: 24 JUL 2013 11:33AM EST
- Manuscript Revised: 17 JUL 2013
- Manuscript Accepted: 17 JUL 2013
- Manuscript Received: 23 MAY 2013
- National Institutes of Health. Grant Numbers: R01EY015518, R21DC010912
- Children's Hospital of Wisconsin (EVS)
- Clinical and Translational Science Award (CTSA) program. Grant Number: 1UL1RR031973
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