Correspondence on "Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder" by Cuinat et al

Genet Med. 2023 Sep;25(9):100878. doi: 10.1016/j.gim.2023.100878. Epub 2023 Jun 5.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Humans
  • Mutation
  • Neurodevelopmental Disorders* / genetics
  • RNA-Binding Proteins / genetics

Substances

  • SRRM2 protein, human
  • RNA-Binding Proteins