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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...
Autores principales: | Drozd, Małgorzata, Bardoni, Barbara, Capovilla, Maria |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
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 |
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