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Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females
- Correspondence to Dr C Philippe, Laboratoire de Génétique Médicale, Nancy Université, EA 4002, Centre Hospitalier Régional et Universitaire, Rue du Morvan, 54511 cedex 1, Vandoeuvre-les-Nancy, France; c.philippe{at}chu-nancy.fr
Citation
Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females
Publication history
- Received February 24, 2009
- Revised April 20, 2009
- Accepted April 29, 2009
- First published June 29, 2009.
Online issue publication
April 27, 2016
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© 2009, Published by the BMJ Publishing Group Limited For permission to use, (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.