Relevant conflicts of interest/financial disclosures: Nothing to report.
Letters: New Observations
A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder
Version of Record online: 13 FEB 2013
Copyright © 2013 Movement Disorders Society
Volume 28, Issue 4, pages 559–560, April 2013
How to Cite
Manganelli, F., Dubbioso, R., Esposito, M., Marinò, C., Pisciotta, C., Pignatelli, S. and Santoro, L. (2013), A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder. Mov. Disord., 28: 559–560. doi: 10.1002/mds.25308
Full financial disclosures and author roles may be found in the online version of this article.
- Issue online: 8 APR 2013
- Version of Record online: 13 FEB 2013
- Manuscript Accepted: 5 NOV 2012
- Manuscript Revised: 29 OCT 2012
- Manuscript Received: 29 AUG 2012
Supporting Information may be found in the online version of this article.
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