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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Detalles Bibliográficos
Autores principales: Zhang, Jiang, Wang, Guangli, He, Wei-Wu, Losh, Molly, Berry-Kravis, Elizabeth, Funk, William E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399764/
https://www.ncbi.nlm.nih.gov/pubmed/30853789
http://dx.doi.org/10.1177/1178641818825268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399764/
https://www.ncbi.nlm.nih.gov/pubmed/30853789
http://dx.doi.org/10.1177/1178641818825268

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