The Identification of Nuclear FMRP Isoform Iso6 Partners
A deficiency of FMRP, a canonical RNA-binding protein, causes the development of Fragile X Syndrome (FXS), which is characterised by multiple phenotypes, including neurodevelopmental disorders, intellectual disability, and autism. Due to the alternative splicing of the encoding <i>FMR1</i&g...
| Glavni autori: | , , , , , , |
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| Format: | Članak |
| Jezik: | English |
| Izdano: |
MDPI AG
2023-12-01
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| Serija: | Cells |
| Teme: | |
| Online pristup: | https://www.mdpi.com/2073-4409/12/24/2807 |