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
R. Galluzzi
S. M. Bacca
R. Giorda
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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vol. 67 no. 5 867-868
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History:
- First Published September 11, 2006.
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© 2006
Author Disclosures
- P. Ventura, MD,
- R. Galluzzi, MD,
- S. M. Bacca, MD,
- R. Giorda, PhD and
- A. Massagli, MD
- P. Ventura, MD,
- R. Galluzzi, MD,
- S. M. Bacca, MD,
- R. Giorda, PhD and
- A. Massagli, MD
- 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.
- 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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