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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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| 出版年: | Acta Biochim Biophys Sin (Shanghai) |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2014
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| 主題: | |
| オンライン･アクセス: | 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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