Modeling Fragile X Syndrome in Drosophila

Intellectual disability (ID) and autism are hallmarks of Fragile X Syndrome (FXS), a hereditary neurodevelopmental disorder. The gene responsible for FXS is Fragile X Mental Retardation gene 1 (FMR1) encoding the Fragile X Mental Retardation Protein (FMRP), an RNA-binding protein involved in RNA met...

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Detalles Bibliográficos
Autores principales: Drozd, Małgorzata, Bardoni, Barbara, Capovilla, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911982/
https://www.ncbi.nlm.nih.gov/pubmed/29713264
http://dx.doi.org/10.3389/fnmol.2018.00124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911982/
https://www.ncbi.nlm.nih.gov/pubmed/29713264
http://dx.doi.org/10.3389/fnmol.2018.00124

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