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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome
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  1. Correspondence to:
 Ignatia B Van den Veyver
 Department of Obstetrics and Gynecology, Baylor College of Medicine, 6550 Fannin, Suite 901, Houston, TX, USA; iveyverbcm.tmc.edu
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Citation

Amir RE, Fang P, Yu Z, et al
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

Publication history

  • Accepted October 7, 2004
  • Revised October 7, 2004
  • First published February 2, 2005.
Online issue publication 
February 02, 2005

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