GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model
Fragile X syndrome (FXS), caused by loss of FMR1 gene function, is the most common heritable cause of intellectual disability and autism spectrum disorders. The FMR1 protein (FMRP) translational regulator mediates activity-dependent control of synapses. In addition to the metabotropic glutamate rece...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2014-05-01
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Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996114000151 |