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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cas...

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cas...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2098880890

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Background: Genetic risk for bipolar disorder (BD) is conferred through many common alleles, while a role for rare copy number variants (CNVs) is less clear. BD subtypes schizoaffective disorder bipolar type (SAB), bipolar I disorder (BD I) and bipolar II disorder (BD II) differ according to the prominence and timing of psychosis, mania and depress...

Alternative Titles

Full title

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2098880890

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2098880890

Other Identifiers

ISSN

2692-8205

E-ISSN

2692-8205

DOI

10.1101/406215