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15q13.3 duplication in two patients with childhood‐onset schizophrenia
We report two cases of paternally inherited 15q13.3 duplications in carriers diagnosed with childhood‐onset schizophrenia (COS), a rare neurodevelopmental disorder of proposed polygenic origin with onset in children before age 13. This study documents that the 15q13.3 deletion and duplication exhibi...
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| 發表在: | Am J Med Genet B Neuropsychiatr Genet |
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| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5069586/ https://ncbi.nlm.nih.gov/pubmed/26968334 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32439 |
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