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Archive ouverte | Galy, Anne | CCSD

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Archive ouverte | Abekhoukh, Sabiha | CCSD

International audience. Cytoplasmic FMRP interacting protein 1 (CYFIP1) is a candidate gene for intellectual disability (ID), autism, schizophrenia and epilepsy. It is a member of a family of proteins that is highly...

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Archive ouverte | Reeve, Simon P | CCSD

Fragile X syndrome is the most common form of heritable mental retardation caused by the loss of function of the fragile X mental retardation protein FMRP. FMRP is a multidomain, RNA-binding protein involved in RNA transport and/o...

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