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Bcl-2-associated transcription factor 1 interacts with fragile X-related protein 1
The absence of fragile X mental retardation protein (FMRP) causes fragile X syndrome (FXS), which is the leading cause of hereditary mental retardation. Fragile X-related protein 1 (FXR1P), which plays an important role in normal muscle development, is one of the two autosomal paralogs of FMRP. To u...
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| Publicado no: | Acta Biochim Biophys Sin (Shanghai) |
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| Main Authors: | , , , , , , |
| 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/PMC7109863/ https://ncbi.nlm.nih.gov/pubmed/24389646 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/abbs/gmt134 |
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