Genetic variation in the 22q11 locus and susceptibility to schizophrenia
An increased prevalence of microdeletions at the 22q11 locus has been reported in samples of patients with schizophrenia. 22q11 microdeletions represent the highest known genetic risk factor for the development of schizophrenia, second only to that of the monozygotic cotwin of an affected individual...
שמור ב:
| הוצא לאור ב: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
2002
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC139234/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12477929/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.232186099 |
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