KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism
- 30 September 1993
- journal article
- Published by Elsevier BV in Trends in Biochemical Sciences
- Vol. 18 (9), 331-333
- https://doi.org/10.1016/0968-0004(93)90068-x
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Characterization and localization of the FMR-1 gene product associated with fragile X syndromeNature, 1993
- Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndromeNature Genetics, 1993
- A point mutation in the FMR-1 gene associated with fragile X mental retardationNature Genetics, 1993
- Molecular genetics of the fragile-X syndrome: a novel type of unstable mutationCurrent Opinion in Genetics & Development, 1992
- Fragile X syndrome without CCG amplification has an FMR1 deletionNature Genetics, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 1991
- Prevalence of the fragile‐X syndrome in mentally retarded boys in a Swedish countyAmerican Journal of Medical Genetics, 1986
- Population incidence and segregation ratios in the Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1986