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September 12, 2006; 67 (5) Brief Communications

A novel familial MECP2 mutation in a young boy: Clinical and molecular findings

P. Ventura, R. Galluzzi, S. M. Bacca, R. Giorda, A. Massagli
First published September 11, 2006, DOI: https://doi.org/10.1212/01.wnl.0000233990.87889.15
P. Ventura
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R. Galluzzi
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S. M. Bacca
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R. Giorda
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A. Massagli
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A novel familial MECP2 mutation in a young boy: Clinical and molecular findings
P. Ventura, R. Galluzzi, S. M. Bacca, R. Giorda, A. Massagli
Neurology Sep 2006, 67 (5) 867-868; DOI: 10.1212/01.wnl.0000233990.87889.15

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Article Information

vol. 67 no. 5 867-868
DOI: 
https://doi.org/10.1212/01.wnl.0000233990.87889.15
PubMed: 
16966553

Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published September 11, 2006.

Copyright & Usage: 
© 2006

Author Disclosures

    1. P. Ventura, MD,
    2. R. Galluzzi, MD,
    3. S. M. Bacca, MD,
    4. R. Giorda, PhD and
    5. A. Massagli, MD
  1. P. Ventura, MD,
  2. R. Galluzzi, MD,
  3. S. M. Bacca, MD,
  4. R. Giorda, PhD and
  5. A. Massagli, MD
  1. From the Department of Neurorehabilitation 2 Psychopathological disturbances in childhood and adolescence (P.V., R.G., S.M.B., A.M.), Scientific Institute “Eugenio Medea” for Research, Hospitalization and Healthcare, Regional Branch of Ostuni (BR), Italy; and Molecular Biology Laboratory (R.G.), Scientific Institute “Eugenio Medea” for Research, Hospitalization and Healthcare, Regional Branch of Bosisio Parini (LC), Italy.
  1. Address correspondence and reprint requests to Dr. Angelo Massagli, Department of Neurorehabilitation 2, Scientific Institute “Eugenio Medea,” Regional Branch of Ostuni, Via Dei Colli 7, 72017 Ostuni (BR), Italy; e-mail: address: massagli{at}os.lnf.it
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