A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans

author
created [InstanceEdit:9970097] Orlic-Milacic, Marija, 2025-10-27
dbId 9970099
displayName A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans
journal Nucleic Acids Res
pages 9804-9821
pubMedIdentifier 32816001
schemaClass LiteratureReference
title A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans
url http://www.ncbi.nlm.nih.gov/pubmed/32816001
volume 48
year 2020
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