Llwytho...
Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP
Fragile X syndrome is a monogenic disorder and a common cause of intellectual disability. Despite nearly 25 years of research on FMR1, the gene underlying the syndrome, very few pathological mutations other than the typical CGG-repeat expansion have been reported. This is in contrast to other X-link...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Exp Neurosci |
|---|---|
| Prif Awduron: | , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Libertas Academica
2015
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4720182/ https://ncbi.nlm.nih.gov/pubmed/26819560 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/JEN.S25524 |
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