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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Detalhes bibliográficos
Publicado no:BMC Biol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research Article
Acesso em linha: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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