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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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Bibliographic Details
Main Authors: Cheever, Anne, Blackwell, Ernest, Ceman, Stephanie
Format: Artigo
Language:Inglês
Published: Cold Spring Harbor Laboratory Press 2010
Subjects:
Online Access: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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