FXR1, an autosomal homolog of the fragile X mental retardation gene.

Fragile X mental retardation syndrome, the most common cause of hereditary mental retardation, is directly associated with the FMR1 gene at Xq27.3. FMR1 encodes an RNA binding protein and the syndrome results from lack of expression of FMR1 or expression of a mutant protein that is impaired in RNA b...

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Dades bibliogràfiques
Publicat a:EMBO J
Autors principals: Siomi, M C, Siomi, H, Sauer, W H, Srinivasan, S, Nussbaum, R L, Dreyfuss, G
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 1995
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC398353/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7781595/
https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1995.tb07237.x
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