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De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon‐skipping variant
AIM: We previously performed the first trio‐based exome study for bipolar disorder and identified 71 de novo mutations. Among these mutations, the only mutation located at the splice donor site was in UNC13B. We focused on and analyzed the functions of the mutation. METHODS: In order to analyze the...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292303/ https://www.ncbi.nlm.nih.gov/pubmed/30117296 http://dx.doi.org/10.1002/npr2.12027 |