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...

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Détails bibliographiques
Publié dans:BMC Biol
Auteurs principaux: 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.
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2020
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7493858/
https://ncbi.nlm.nih.gov/pubmed/32938458
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12915-020-00857-6
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