Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations

Although numerous genetic studies have been conducted for bipolar disorder (BD), its genetic architecture remains elusive. Here we perform, to the best of our knowledge, the first trio-based exome sequencing study for BD to investigate potential roles of de novo mutations in the disease etiology. We...

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Detalhes bibliográficos
Publicado no:Mol Psychiatry
Main Authors: Kataoka, M, Matoba, N, Sawada, T, Kazuno, A-A, Ishiwata, M, Fujii, K, Matsuo, K, Takata, A, Kato, T
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
Assuntos:
Immediate Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5414074/
https://ncbi.nlm.nih.gov/pubmed/27217147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2016.69
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