The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.

Fragile X Mental Retardation Syndrome is the most common form of hereditary mental retardation, and is caused by defects in the FMR1 gene. FMR1 is 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 binding. The sp...

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Detalhes bibliográficos
Publicado no:EMBO J
Main Authors: Zhang, Y, O'Connor, J P, Siomi, M C, Srinivasan, S, Dutra, A, Nussbaum, R L, Dreyfuss, G
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 1995
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC394645/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7489725/
https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1995.tb00220.x
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