Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome

Loss or disrupted expression of the FMR1 gene causes fragile X syndrome (FXS), the most common monogenetic form of autism in humans. Although disruptions in sensory processing are core traits of FXS and autism, t...

Source: BMC Biology - September 16, 2020 Category: Biology Authors: Lena Constantin, Rebecca E. Poulsen, Leandro A. Scholz, Itia A. Favre-Bulle, Michael A. Taylor, Biao Sun, Geoffrey J. Goodhill, Gilles C. Vanwalleghem and Ethan K. Scott Tags: Research article Source Type: research