Article

Astroglial FMRP modulates synaptic signaling and behavior phenotypes in FXS mouse model

2020-02-11

Abstract excerpt

Fragile X syndrome (FXS) is one of the most common inherited intellectual disability (ID) disorders, in which the loss of FMRP protein induces a range of cellular signaling changes primarily through excess protein synthesis. Although neuron-centered molecular and cellular events underlying FXS have been characterized, how different CNS cell types are involved in typical FXS synaptic signaling changes and behaviora...

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Literature Corpus work: 8f69d53f-c48f-53f1-9095-1441c3653407
DOI: 10.1101/2020.02.10.941971

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