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HILAL , Fahd

Last name: HILAL

First name: Fahd

September 27, 2022 (v1)

Journal article

Metadata-only

Combining affinity purification and mass spectrometry to define the network of the nuclear proteins interacting with the N-terminal region of FMRP

Kieffer, Félicie Hilal, Fahd Gay, Anne-Sophie

Fragile X-Syndrome (FXS) represents the most common inherited form of intellectual disability and the leading monogenic cause of Autism Spectrum Disorders. In most cases, this disease results from the absence of expression of the protein FMRP encoded by the FMR1 gene (Fragile X messenger ribonucleoprotein 1). FMRP is mainly defined as a...

Uploaded on: December 4, 2022