Article
Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases
2018-09-03
Abstract excerpt
<h4>Background</h4> 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 depression. The factors contributing to the combination of sympto...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 46cd051d-1c6f-54ec-a09b-4e9ebe0f6fff
- DOI
- 10.1101/406215
