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Searching for the true genetic vulnerability for schizophrenia
The search for a genetic basis for schizophrenia has taken a new turn recently with the publication of three reports of various rare copy-number variations that are associated with schizophrenia. While some of the findings may simply disappear as spurious reports, others remain interesting: that is,...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651590/ https://www.ncbi.nlm.nih.gov/pubmed/19348701 http://dx.doi.org/10.1186/gm14 |
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author | DeLisi, Lynn E |
author_facet | DeLisi, Lynn E |
author_sort | DeLisi, Lynn E |
collection | PubMed |
description | The search for a genetic basis for schizophrenia has taken a new turn recently with the publication of three reports of various rare copy-number variations that are associated with schizophrenia. While some of the findings may simply disappear as spurious reports, others remain interesting: that is, deletions in the Velocardiofacial syndrome region of chromosome 22, and regions of chromosome 1q21.1 and 15q13.3. These results will gain greater significance if future validation in family studies shows their segregation with illness within families, and when it is understood how the genes containing these variants affect the underlying neurochemistry and neuropathology characteristic of schizophrenia. |
format | Text |
id | pubmed-2651590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26515902009-03-09 Searching for the true genetic vulnerability for schizophrenia DeLisi, Lynn E Genome Med Minireview The search for a genetic basis for schizophrenia has taken a new turn recently with the publication of three reports of various rare copy-number variations that are associated with schizophrenia. While some of the findings may simply disappear as spurious reports, others remain interesting: that is, deletions in the Velocardiofacial syndrome region of chromosome 22, and regions of chromosome 1q21.1 and 15q13.3. These results will gain greater significance if future validation in family studies shows their segregation with illness within families, and when it is understood how the genes containing these variants affect the underlying neurochemistry and neuropathology characteristic of schizophrenia. BioMed Central 2009-01-23 /pmc/articles/PMC2651590/ /pubmed/19348701 http://dx.doi.org/10.1186/gm14 Text en Copyright ©2009 BioMed Central Ltd |
spellingShingle | Minireview DeLisi, Lynn E Searching for the true genetic vulnerability for schizophrenia |
title | Searching for the true genetic vulnerability for schizophrenia |
title_full | Searching for the true genetic vulnerability for schizophrenia |
title_fullStr | Searching for the true genetic vulnerability for schizophrenia |
title_full_unstemmed | Searching for the true genetic vulnerability for schizophrenia |
title_short | Searching for the true genetic vulnerability for schizophrenia |
title_sort | searching for the true genetic vulnerability for schizophrenia |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2651590/ https://www.ncbi.nlm.nih.gov/pubmed/19348701 http://dx.doi.org/10.1186/gm14 |
work_keys_str_mv | AT delisilynne searchingforthetruegeneticvulnerabilityforschizophrenia |