Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients.

Abstract

Large rare deletions in NRXN1 increase the risk for schizophrenia. The aim of the present study was to determine whether small rare sequence changes in exons and splice sites contribute to the development of schizophrenia in a high-penetrance manner. Complete coding regions and splice sites were resequenced in 94 patients and 94 controls. Among the 16 rare… (More)
DOI: 10.1016/j.schres.2011.01.001

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