Identification of ultra-rare missense mutations associated with familial schizophrenia by whole-exome sequencing

Schizophr Res. 2021 Sep:235:60-62. doi: 10.1016/j.schres.2021.07.027. Epub 2021 Jul 26.
No abstract available

Publication types

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

MeSH terms

  • Exome / genetics
  • Exome Sequencing
  • Genetic Predisposition to Disease
  • Humans
  • Mutation
  • Mutation, Missense*
  • Pedigree
  • Schizophrenia* / genetics