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How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
The 22q11.2 deletion syndrome is caused by a microdeletion of chromosome 22. One third of all patients with 22q11.2 deletion develop schizophrenia-like symptoms. In general, the prevalence of 22q11.2 deletion in patients with schizophrenia is 1%–2%. The 22q11.2 deletion is one of the major known gen...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3849181/ https://ncbi.nlm.nih.gov/pubmed/24063534 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-859X-12-29 |
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