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New Perspectives on the Biology of Fragile X Syndrome
Fragile X syndrome (FXS) is a trinucleotide repeat disorder caused by a CGG repeat expansion in FMR1, and loss of its protein product FMRP. Recent studies have provided increased support for the role of FMRP in translational repression via ribosomal stalling and the microRNA pathway. In neurons, par...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3653273/ https://ncbi.nlm.nih.gov/pubmed/22382129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2012.02.002 |
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