Evidence for association between novel polymorphisms in thePRODH gene and schizophrenia in a Chinese population
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference21 articles.
1. Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population
2. Twin studies of schizophrenia: From bow-and-arrow concordances to Star Wars Mx and functional genomics
3. A common molecular basis for rearrangement disorders on chromosome 22q11
4. A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population
5. The gene encoding proline dehydrogenase modulates sensorimotor gating in mice
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