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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
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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 
January 11, 2010

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