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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...

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Literature Corpus work
46cd051d-1c6f-54ec-a09b-4e9ebe0f6fff
DOI
10.1101/406215
Open publication

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Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective casesDOI 10.1101/406215
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