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CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size
Large expansions of a CGG-repeat element (>200 repeats; full mutation) in the fragile X mental retardation 1 (FMR1) gene cause fragile X syndrome (FXS), the leading single-gene form of intellectual disability and of autism spectrum disorder. Smaller expansions (55–200 CGG repeats; premutation) re...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4030777/ https://ncbi.nlm.nih.gov/pubmed/24463622 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu032 |
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