A chromosome 16p13.11 microduplication causes hyperactivity through dysregulation of miR-484/protocadherin-19 signaling

Chromosome 16p13.11 microduplication is a risk factor associated with various neurodevelopmental disorders such as attention-deficit/hyperactivity disorder, intellectual disabilities, developmental delay and autistic spectrum disorder. The underlying molecular mechanism of this genetic variation rem...

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Detalles Bibliográficos
Autores principales: Fujitani, M, Zhang, S, Fujiki, R, Fujihara, Y, Yamashita, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322274/
https://www.ncbi.nlm.nih.gov/pubmed/27378146
http://dx.doi.org/10.1038/mp.2016.106

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322274/
https://www.ncbi.nlm.nih.gov/pubmed/27378146
http://dx.doi.org/10.1038/mp.2016.106

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