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Angelman syndrome phenotype associated with mutations inMECP2, a gene encoding a methyl CpG binding protein
  1. Dr Clayton-Smith,Jcs{at}central.cmht.nwest.nhs.uk
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Citation

Watson P, Black G, Ramsden S, et al
Angelman syndrome phenotype associated with mutations inMECP2, a gene encoding a methyl CpG binding protein

Publication history

  • Revised January 12, 2001
  • Accepted January 13, 2001
  • First published April 1, 2001.
Online issue publication 
April 27, 2016

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