RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability

Brain. 2020 Apr 1;143(4):e31. doi: 10.1093/brain/awaa070.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Female
  • Genes, Recessive
  • Humans
  • Intellectual Disability / genetics*
  • Loss of Function Mutation
  • Male
  • Nuclear Proteins / genetics*

Substances

  • Nuclear Proteins
  • RSRC1 protein, human