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pro vyhledávání: '"Caill√©, I."'
Autor:
Messaoudi, S., Stoufflet, J., Fouquet, C., Doulazmi, M., Allam, A., Paillard, T., Trembleau, A., Caillé, I.
Publikováno v:
bioRxiv
The Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability, and the first monogenic cause of Autism Spectrum Disorder. FXS is caused by the absence of the RNA-binding protein FMRP (Fragile X Mental Retardation Protein).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba7bbf76e86d4a2927b95207b0d9b474
https://europepmc.org/articles/PMC10028813/
https://europepmc.org/articles/PMC10028813/
