| Literature DB >> 16389584 |
Hélène Jacquet1, Judith L Rapoport, Bernadette Hecketsweiler, Aaron Bobb, Florence Thibaut, Thierry Frébourg, Dominique Campion.
Abstract
In a previous report [Jacquet et al., 2005] we have shown that mild to moderate hyperprolinemia resulting from several alterations (either a complete deletion or missense mutations) of the proline dehydrogenase (PRODH) gene located on chromosome 22q11 is a risk factor for schizoaffective disorder but not for DSM3 R schizophrenia or bipolar disorder. We now report that hyperprolinemia is not associated with childhood onset schizophrenia (COS).Entities:
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Year: 2006 PMID： 16389584 DOI： 10.1002/ajmg.b.30263
Source DB: PubMed Journal: Am J Med Genet B Neuropsychiatr Genet ISSN： 1552-4841 Impact factor: 3.568