AAV-mediated FOXG1 gene editing in human Rett primary cells

Croci, S; Carriero, ML; Capitani, K; Daga, S; Donati, F; Papa, FT; Frullanti, E; Lopergolo, D; Lamacchia, V; Tita, R; Giliberti, A; Benetti, E; Niccheri, F; Furini, S; Lo Rizzo, C; Conticello, SG; Renieri, A; Meloni, I

Renieri, A (corresponding author), Univ Siena, Med Genet, Siena, Italy.; Renieri, A (corresponding author), Azienda Osped Univ Senese, Genet Med, Siena, Italy.

EUROPEAN JOURNAL OF HUMAN GENETICS, 2020; 28 (10): 1446

Abstract

Variations in theForkhead Box G1(FOXG1)gene causeFOXG1syndrome spectrum, including the congenital variant of Rett syndrome, characterized by early ons......

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