Rare loss-of-function variants in HECTD2 and AKAP11 confer a risk of bipolar disorder
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deCODE genetics  
March 25, 2025

Rare loss-of-function variants in HECTD2 and AKAP11 confer a risk of bipolar disorder

Scientists at deCODE genetics, a subsidiary of Amgen, reveal today in Nature Genetics associations between rare loss-of-function variants in two genes and bipolar disorder.

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