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Autor:
Jessica L. Huebschman, Carolina A. Monterrey, Dorothy M. Foster, Chris C. Omoregie, Alp E. Cakir, Adrian Sevilla-Gutierrez, Elsbeth C. Chow, Amanda Essoh, Yuhong Guo, Laura N. Smith
Publikováno v:
Brain research. 1795
Fragile X syndrome (FXS), a leading monogenic cause of autism spectrum disorders (ASDs), typically occurs as the result of a mutation silencing the Fmr1 gene, preventing production of the fragile X messenger ribonucleoprotein (FMRP). FXS is character