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Paper Details

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
JAMA Psychiatry
110
2013
2q22 region, GRM5, LRP1B, N -methyl-D-aspartate, N-methyl-D-aspartate, N-methyl-D-aspartate receptor, NMDA, NMDA receptor, PARTICIPANTS, PPEF2, Schizophrenia, calmodulin-binding protein phosphatase, copy number variants, cultured cells, genetic disorder, genetic factors, glutamate, inherited disease, low-density lipoprotein receptor-related protein, mGluR5, metabotropic glutamate receptor subtype 5, schizophrenia, tamalin
Author NameAffiliation
Andrew E TimmsUniversity of Washington School of Medicine
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Datasets

Release 1.2