Towards Mechanism-based Treatments for Fragile X Syndrome
It has been more than 25 years since the identification of the FMR1 gene and the demonstration of the causative role of CGG-repeat expansion in the disease pathology of fragile X syndrome (FXS), but the underlying mechanisms involved in the expansion mutation and the resulting gene silencing still r...
| Format: | eBook |
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| Language: | English |
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MDPI - Multidisciplinary Digital Publishing Institute
2019
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| Online Access: | Open Access: DOAB: description of the publication Open Access: DOAB, download the publication |