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Fragile X protein family member FXR1P is regulated by microRNAs
FXR1P is one of two autosomal paralogs of the fragile X mental retardation protein FMRP. The absence of FMRP causes fragile X syndrome, the leading cause of hereditary mental retardation. FXR1P plays an important role in normal muscle development and has been implicated in facioscapulohumeral muscul...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2010
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2905753/ https://ncbi.nlm.nih.gov/pubmed/20519410 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.2022210 |
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