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Autor:
Giorgio, Pini, Stefania, Bigoni, Ingegerd Witt, Engerström, Olga, Calabrese, Beatrice, Felloni, Maria Flora, Scusa, Pietro, Di Marco, Paolo, Borelli, Ubaldo, Bonuccelli, Peter O O, Julu, Jytte Bieber, Nielsen, Bodil, Morin, Stig, Hansen, Giuseppe, Gobbi, Paola, Visconti, Maria, Pintaudi, Veneselli, Edvige, Anna, Romanelli, Fabrizio, Bianchi, Manuela, Casarano, Roberta, Battini, Giovanni, Cioni, Francesca, Ariani, Alessandra, Renieri, Alberto, Benincasa, Robert S, Delamont, Michele, Zappella, Eric E J, Smeets
Publikováno v:
Neuropediatrics, 43(1), 37-43. Georg Thieme Verlag
Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively females. The Hanefeld variant, or early-onset seizure variant, has been associated with mutations in CDKL5 gene.In recent years more than 60 patients with mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0409f97ebac9c4fbd6e76388ad1f213
http://hdl.handle.net/11568/202217
http://hdl.handle.net/11568/202217
