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Keep this study
Lead
Hôpital le Vinatier
The main objective of the study is to propose a whole exome sequencing (WES), pan-genomic in whole genome sequencing (WGS), transcriptomic, epigenomic and intestinal microbiome approaches in order to determine specific molecular basis of psychotic symptoms in 22q11.2DS.
Age
18–45
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
• Sisterhood of monozygotic twins diagnosed with de novo 22q11.2DS is confirmed by CGH array and discordant for the psychiatric phenotype
You may not be if
• Refusal to use data for research purposes
Clareo Health | Molecular Variants Associated With Schizophrenia: Differential Analysis of Monozygotic Twins With Variable Phenotypic 22q11
