Communicated by Maria Rita Passos-Bueno
PCDH19-related infantile epileptic encephalopathy: An unusual X-linked inheritance disorder†
Article first published online: 14 FEB 2012
© 2012 Wiley Periodicals, Inc.
Special Issue: Focus on the NIH Undiagnosed Diseases Program
Volume 33, Issue 4, pages 627–634, April 2012
How to Cite
Depienne, C. and LeGuern, E. (2012), PCDH19-related infantile epileptic encephalopathy: An unusual X-linked inheritance disorder. Hum. Mutat., 33: 627–634. doi: 10.1002/humu.22029
- Issue published online: 12 MAR 2012
- Article first published online: 14 FEB 2012
- Accepted manuscript online: 20 JAN 2012 12:00AM EST
- Manuscript Accepted: 10 JAN 2012
- Manuscript Received: 4 OCT 2011
- GIS Maladies rares, Assistance Publique des hôpitaux de Paris including the Programme Hospitalier de Recherche Clinique (#P020910/AOR02085), Institut National de la Santé et de la Recherche Médicale, and Université Pierre et Marie-Curie
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