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Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Eduardo A Maury1,2,3, Maxwell A Sherman4, Giulio Genovese3,5,6

  • 1Division of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children's Hospital, Boston, MA, USA.

Cell Genomics
|August 21, 2023
PubMed

Keywords:
ABCB11NRXN1genomicsmosaicismschizophreniasomaticstructural variantstreatment resistance

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