In vivo dissection of human NRXN1 isoforms reveals gain-of-function pathogenicity of schizophrenia-associated 3' deletions
Dustin Haskell, Michael P. Hart
The paper expresses human NRXN1 isoforms in C. elegans to assess their functional impact, finding that some 3' deletion variants cause gain-of-function pathogenicity in behavior.
Human Molecular Genetics · Jan 1, 2026Peer-reviewedNeuroscience