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December 2014 (v1)Journal articleUploaded on: December 4, 2022
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December 2014 (v1)Journal article
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Uploaded on: December 4, 2022 -
December 2014 (v1)Journal article
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Uploaded on: February 22, 2023 -
February 22, 2018 (v1)Journal article
Fragile X syndrome (FXS) is the most frequent inherited cause of intellectual disability and the best-studied monogenic cause of autism. FXS results from the functional absence of the fragile X mental retardation protein (FMRP) leading to abnormal pruning and consequently to synaptic communication defects. Here we show that FMRP is a substrate...
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December 2018 (v1)Journal article
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Uploaded on: February 22, 2023 -
December 2018 (v1)Journal article
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Uploaded on: December 4, 2022 -
December 2018 (v1)Journal article
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Uploaded on: February 22, 2023 -
December 14, 2020 (v1)Publication
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. FXS is usually caused by a CGG-repeat expansion in the FMR1 gene leading to its silencing and the loss-of-expression of the Fragile X Mental Retardation Protein (FMRP). Missense mutations were also identified...
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December 2018 (v1)Journal article
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Uploaded on: December 4, 2022 -
March 10, 2021 (v1)Journal article
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. CGG-repeat expansion in the FMR1 gene leads to FMR1 silencing, loss-of-expression of the Fragile X Mental Retardation Protein (FMRP), and is a common cause of FXS. Missense mutations in the FMR1 gene were...
Uploaded on: December 4, 2022 -
October 2015 (v1)Journal article
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Uploaded on: December 4, 2022