Erratum: Variant of rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238))

Giorgio Pini, Stefania Bigoni, Ingegerdwitt Engerström, Olga Calabrese, Beatrice Felloni, Mariaflora Scusa, Pietro Di Marco, Paolo Borelli, Ubaldo Bonuccelli, Petero O. Julu, Jyttebieber Nielsen, Bodil Morin, Stig Hansen, Giuseppe Gobbi, Paola Visconti, Maria Pintaudi, Veneselli Edvige, Anna Romanelli, Fabrizio Bianchi, Manuela CasaranoRoberta Battini, Giovanni Cioni, Francesca Ariani, Alessandra Renieri, Alberto Benincasa, Roberts Delamont, Michele Zappella

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)237
Number of pages1
JournalNeuropediatrics
Volume44
Issue number4
DOIs
Publication statusPublished - 2013

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

Cite this

Pini, G., Bigoni, S., Engerström, I., Calabrese, O., Felloni, B., Scusa, M., Di Marco, P., Borelli, P., Bonuccelli, U., Julu, P. O., Nielsen, J., Morin, B., Hansen, S., Gobbi, G., Visconti, P., Pintaudi, M., Edvige, V., Romanelli, A., Bianchi, F., ... Zappella, M. (2013). Erratum: Variant of rett syndrome and CDKL5 gene: Clinical and autonomic description of 10 cases (Neuropediatrics (2013) 44 (237-238)). Neuropediatrics, 44(4), 237. https://doi.org/10.1055/s-0033-1343839