Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

This publication has 35 references indexed in Scilit:

• KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism
  Trends in Biochemical Sciences, 1993
• Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat
  Nature Genetics, 1993
• hnRNP PROTEINS AND THE BIOGENESIS OF mRNA
  Annual Review of Biochemistry, 1993
• Enhanced Fmr–1 expression in testis
  Nature Genetics, 1993
• Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
  Nature Genetics, 1993
• A point mutation in the FMR-1 gene associated with fragile X mental retardation
  Nature Genetics, 1993
• Complete cDNA sequence of chicken vigilin, a novel protein with amplified and evolutionary conserved domains
  European Journal of Biochemistry, 1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Absence of expression of the FMR-1 gene in fragile X syndrome
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991