| 摘要 |
The present invention relates to association of one or more polymorphisms located in the human NHP2L1 , PACSIN2, SERHL, PIPPIN, BRD1 , EP300, FAM19A5 and/or GPR24 genes to the occurrence of schizophrenia and/or bipolar disorder. The invention relates both to methods for diagnosing a predisposition to said diseases and for treating subjects having said diseases. |
| 申请人 |
AARHUS UNIVERSITET;REGION MIDTJYLLAND;BOERGLUM, ANDERS;SEVERINSEN, JACOB;MORS, OLE;MUIR, WALTER;BLACKWOOD, DOUGLAS |
发明人 |
BOERGLUM, ANDERS;SEVERINSEN, JACOB;MORS, OLE;MUIR, WALTER;BLACKWOOD, DOUGLAS;EWALD, HENRIK |
