Cargando…

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

BACKGROUND: 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, the neural underpinnings of these phenotypes are poorly understood. Using cal...

Descripción completa

Detalles Bibliográficos
Autores principales: Constantin, Lena, Poulsen, Rebecca E., Scholz, Leandro A., Favre-Bulle, Itia A., Taylor, Michael A., Sun, Biao, Goodhill, Geoffrey J., Vanwalleghem, Gilles C., Scott, Ethan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493858/
https://www.ncbi.nlm.nih.gov/pubmed/32938458
http://dx.doi.org/10.1186/s12915-020-00857-6