A mutation in the DRDS receptor gene has been reported in association with schizophrenia in Japanese and Caucasian populations. The variation, Ser to Cys at codon 311, occurs in the third intracellular loop of the receptor and is therefore putatively functional. W e report the results of screening U
Hyperprolinemia is not associated with childhood onset schizophrenia
✍ Scribed by Hélène Jacquet; Judith L. Rapoport; Bernadette Hecketsweiler; Aaron Bobb; Florence Thibaut; Thierry Frébourg; Dominique Campion
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 40 KB
- Volume
- 141B
- Category
- Article
- ISSN
- 1552-4841
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