학술논문
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development
Document Type
Article
Author
Mazel, B.; Delanne, J.; Garde, A.; Racine, C.; Thauvin-Robinet, C.; Faivre, L.; Bruel, A.-L.; Duffourd, Y.; Philippe, C.; Lopergolo, D.; Santorelli, F.M.; Marchi, V.; Pinto, A.M.; Mencarelli, M.A.; Mari, F.; Renieri, A.; Canitano, R.; Valentino, F.; Papa, F.T.; Fallerini, C.; Munnich, A.; Niclass, T.; Le Guyader, G.
Source
In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics . (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, September 2024, 195(6))
Subject
Language
English
ISSN
1552485X
15524841
15524841