Llwytho...
Examination of FMR1 transcript and protein levels among 74 premutation carriers
Fragile X-associated disorders are caused by a CGG trinucleotide repeat expansion in the 5′-untranslated region of the FMR1 gene. Expansion of the CGG trinucleotide repeats to >200 copies (that is, a full mutation) induces methylation of the FMR1 gene, with transcriptional silencing being the eve...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2009
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4122982/ https://ncbi.nlm.nih.gov/pubmed/19927162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2009.121 |
| Tagiau: |
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