Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]

✍ Scribed by Vacca, Marcella; Filippini, Francesco; Budillon, Alberta; Rossi, Valeria; Ragione, Floriana Della; De Bonis, Maria Luigia; Mercadante, Grazia; Manzati, Elisa; Gualandi, Francesca; Bigoni, Stefania; Trabanelli, Cecilia; Pini, Giorgio; Calzolari, Elisa; Ferlini, Alessandra; Meloni, Ilaria; Hayek, Giuseppe; Zappella, Michele; Renieri, Alessandra; D’Urso, Michele; D’Esposito, Maurizio; Macdonald, Fiona; Kerr, Alison; Dhanjal, Seema; Hulten, Maj

• Book ID: 123485918
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 65 KB
• Volume: 34
• Category: Article
• ISSN: 0387-7604
• DOI: 10.1016/j.braindev.2012.09.010