FOXG1 Variants Can Be Associated with Milder Phenotypes Than Congenital Rett Syndrome with Unassisted Walking and Language Development.
Benoit Mazel,Julian Delanne,Aurore Garde,Caroline Racine,Ange-Line Bruel,Yannis Duffourd,Diego Lopergolo,Filippo Maria Santorelli,Viviana Marchi,Anna Maria Pinto,Maria Antonietta Mencarelli,Roberto Canitano,Floriana Valentino,Filomena Tiziana Papa,Chiara Fallerini,Francesca Mari,Alessandra Renieri,Arnold Munnich,Tanguy Niclass,Gwenael Le Guyader,Christel Thauvin-Robinet,Christophe Philippe,Laurence Faivre AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS（2024）
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congenital Rett syndrome,FOXG1 gene,FOXG1 phenotype spectrum,mild phenotype
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