These authors contributed equally to this work.
Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene
Version of Record online: 9 SEP 2013
© 2013 Wiley Periodicals, Inc.
Volume 31, Issue 1, pages 83–87, January/February 2014
How to Cite
Nanda, A., Pasternack, S. M., Mahmoudi, H., Ishorst, N., Grimalt, R. and Betz, R. C. (2014), Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene. Pediatric Dermatology, 31: 83–87. doi: 10.1111/pde.12219
- Issue online: 7 JAN 2014
- Version of Record online: 9 SEP 2013
- German Research Foundation
|pde12219-sup-0001-TableS1.doc||Word document||58K||Table S1. Comparison of the salient clinical features of the present WSS patients with those from earlier reports.|
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