These authors contributed equally to this work.
An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis
Version of Record online: 18 SEP 2012
© 2012 John Wiley & Sons A/S
Volume 14, Issue 6, pages 466–472, September 2013
How to Cite
An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis., , , , , , .
- Issue online: 19 AUG 2013
- Version of Record online: 18 SEP 2012
- Manuscript Accepted: 2 AUG 2012
- Manuscript Revised: 12 JUL 2012
- Manuscript Received: 7 MAY 2012
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