Expression and Characterization of Human Fragile X Mental Retardation Protein Isoforms and Interacting Proteins in Human Cells

Fragile X mental retardation protein is an mRNA-binding protein associated with phenotypic manifestations of fragile X syndrome, an X-linked disorder caused by mutation in the FMR1 gene that is the most common inherited cause of intellectual disability. Despite the well-studied genetic mechanism of...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Proteomics Insights
Asıl Yazarlar: Zhang, Jiang, Wang, Guangli, He, Wei-Wu, Losh, Molly, Berry-Kravis, Elizabeth, Funk, William E
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: SAGE Publications 2019
Konular:
Original Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6399764/
https://ncbi.nlm.nih.gov/pubmed/30853789
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1178641818825268
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