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Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain
Fragile X syndrome, a common cause of intellectual disability and autism, is due to mutational silencing of the FMR1 gene leading to the absence of its gene product, fragile X mental retardation protein (FMRP). FMRP is a selective RNA binding protein owing to two central K-homology domains and a C-t...
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| Udgivet i: | Hum Mol Genet |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4381759/ https://ncbi.nlm.nih.gov/pubmed/25416280 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu586 |
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