학술논문
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development
Document Type
Journal
Author
Mazel, Benoit; Delanne, Julian; Garde, Aurore; Racine, Caroline; Bruel, Ange-Line; Duffourd, Yannis; Lopergolo, Diego; Santorelli, Filippo Maria; Marchi, Viviana; Pinto, Anna Maria; Mencarelli, Maria Antonietta; Canitano, Roberto; Valentino, Floriana; Papa, Filomena Tiziana; Fallerini, Chiara; Mari, Francesca; Renieri, Alessandra; Munnich, Arnold; Niclass, Tanguy; Le Guyader, Gwenael; Thauvin-Robinet, Christel; Philippe, Christophe; Faivre, Laurence
Source
Subject
Language
English
ISSN
1552485X