Authors of Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder (IMAGE)

deCODE genetics

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

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Kari Stefansson CEO of deCODE genetics  withThorgeir Thorgeirsson and Vinicius Tragante, scientists at deCODE genetics and authors of  Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder

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deCODE genetics

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