A novel co-segregating DCTN1 splice site variant in a family with Bipolar Disorder may hold the key to understanding the etiology
André Hallen, Arthur J.L. Cooper
A novel DCTN1 splice site variant was identified in a family with bipolar disorder and major depressive disorder, potentially causing neuronal dysfunction through altered splicing and protein truncation.
Genes · Apr 18, 2020Peer-reviewedGenetics