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Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila
Fragile X syndrome (FXS), the most common inherited determinant of intellectual disability and autism spectrum disorders, is caused by loss of the fragile X mental retardation 1 (FMR1) gene product (FMRP), an mRNA-binding translational repressor. A number of conserved FMRP targets have been identifi...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
The Company of Biologists Limited
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3820263/ https://ncbi.nlm.nih.gov/pubmed/24046358 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.012229 |
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