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The fragile X mental retardation protein inhibits translation via interacting with mRNA

Fragile X syndrome is a frequent form of inherited mental retardation caused by functional loss of the fragile X mental retardation protein, FMRP. The function of FMRP is unknown, as is the mechanism by which its loss leads to cognitive deficits. Recent studies have determined that FMRP is a selecti...

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Detalhes bibliográficos
Main Authors: Li, Zhenzhong, Zhang, Youyi, Ku, Li, Wilkinson, Keith D., Warren, Stephen T., Feng, Yue
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2001
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC55699/
https://ncbi.nlm.nih.gov/pubmed/11376146
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