The Association of V427M Missense Mutation of the PRODH Gene with Schizophrenia in the Iranian Patients
Author:
Publisher
Briefland
Subject
General Medicine
Reference30 articles.
1. Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
2. Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives
3. Assessment of 22q11.2 copy number variations in a sample of Brazilian schizophrenia patients
4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
5. Functional Consequences of PRODH Missense Mutations
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