Article info

Download PDFPDF
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome
  1. Correspondence to Alessandra Renieri, Medical Genetics, Molecular Biology Department, University of Siena, Viale Bracci, 2, 53100 Siena, Italy; renieri{at}unisi.it
View Full Text

Citation

Mencarelli MA, Spanhol-Rosseto A, Artuso R, et al
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome

Publication history

  • Received March 16, 2009
  • Revised May 21, 2009
  • Accepted May 30, 2009
  • First published July 2, 2009.
Online issue publication 
April 27, 2016

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.