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The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders
Over the last fifteen years it has become established that 22q11.2 deletion syndrome (22q11DS) is a true genetic risk factor for schizophrenia. Carriers of deletions in chromosome 22q11.2 develop schizophrenia at rate of 25–30% and such deletions account for as many as 1–2% of cases of sporadic schi...
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| Päätekijät: | , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3074020/ https://ncbi.nlm.nih.gov/pubmed/20920576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijdevneu.2010.09.007 |
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