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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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Detalles Bibliográficos
Autor principal: DeLisi, Lynn E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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.
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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
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