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Singleton deletions throughout the genome increase risk of bipolar disorder

Singleton deletions throughout the genome increase risk of bipolar disorder

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2735188

Singleton deletions throughout the genome increase risk of bipolar disorder

About this item

Full title

Singleton deletions throughout the genome increase risk of bipolar disorder

Publisher

London: Nature Publishing Group UK

Journal title

Molecular psychiatry, 2009-04, Vol.14 (4), p.376-380

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

An overall burden of rare structural genomic variants has not been reported in bipolar disorder (BD), although there have been reports of cases with microduplication and microdeletion. Here, we present a genome-wide copy number variant (CNV) survey of 1001 cases and 1034 controls using the Affymetrix single nucleotide polymorphism (SNP) 6.0 SNP and...

Alternative Titles

Full title

Singleton deletions throughout the genome increase risk of bipolar disorder

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2735188

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2735188

Other Identifiers

ISSN

1359-4184

E-ISSN

1476-5578

DOI

10.1038/mp.2008.144

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