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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Acta Biochim Biophys Sin (Shanghai)
Egile Nagusiak: Ma, Yun, Wang, Changbo, Li, Binyuan, Qin, Lingxue, Su, Jiao, Yang, Manjun, He, Shuya
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2014
Gaiak:
Original Articles
Sarrera elektronikoa: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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