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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Detalles Bibliográficos
Autores principales: Zhou, Dale, Gochman, Peter, Broadnax, Diane D., Rapoport, Judith L., Ahn, Kwangmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069586/
https://www.ncbi.nlm.nih.gov/pubmed/26968334
http://dx.doi.org/10.1002/ajmg.b.32439

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069586/
https://www.ncbi.nlm.nih.gov/pubmed/26968334
http://dx.doi.org/10.1002/ajmg.b.32439

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