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Article

From wings to whiskers to stem cells: why every model matters in fragile X syndrome research

Fragile X syndrome (FXS) is caused by epigenetic silencing of the X-linked fragile X messenger ribonucleoprotein 1 (FMR1) gene located on chromosome Xq27.3, which leads to the loss of its protein product, fragile...

Soraya O. Sandoval, Natasha M. Méndez-Albelo… in Journal of Neurodevelopmental Disorders (2024)