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

Medicine & Life Sciences

• Heterogeneous-Nuclear Ribonucleoprotein K 100%
• RNA-Binding Motifs 83%
• Fragile X Syndrome 77%
• RNA 41%
• Intellectual Disability 37%
• Mutation 33%
• Conserved Sequence 24%
• RNA-Binding Proteins 23%
• RNA Precursors 22%
• Mutant Proteins 21%
• Mutagenesis 19%
• Carrier Proteins 16%
• Genes 8%

Chemical Compounds

• Mutation 50%
• Protein 24%