High Frequency of CNV Mutations in Combined Schizophrenia and Epilepsy
Source: NCBI BioProject (ID PRJNA130899)
Source: NCBI BioProject (ID PRJNA130899)
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Project name: Homo sapiens
Description: Agilent custom designed array comparative genomic hybridization (CGH) was performed on 235 samples with a dual diagnosis of schizophrenia and epilepsy and 80 samples with a dual diagnosis of bipolar and epilpsy. ArrayCGH on 191 psychiatric screened controls was also performed. A common male reference was used for all samples and controls. Samples and controls were obtained from the NIMH cell line repositories.Overall design: 235 samples with a dual diagnosis of schizophrenia and epilepsy, 80 samples with a dual diagnosis of bipolar and epilepsy, and 191 psychiatric screened controls
Data type: Variation
Sample scope: Multiisolate
Relevance: Medical
Organization: Dr. Arthur Beaudet, Molecular and Human Genetics, Baylor College of Medicine
Release date: 2010-12-31
Last updated: 2010-08-18