Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia

Attention deficit hyperactivity disorder (ADHD) is a common and highly heritable neurodevelopmental disorder with poorly understood pathophysiology and genetic mechanisms. A balanced chromosomal translocation interrupts CTNND2 in several members of a family with profound attentional deficit and myop...

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Detalles Bibliográficos
Autores principales: Adegbola, Abidemi, Lutz, Richard, Nikkola, Elina, Strom, Samuel P., Picker, Jonathan, Wynshaw-Boris, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948131/
https://www.ncbi.nlm.nih.gov/pubmed/33718894
http://dx.doi.org/10.1016/j.xhgg.2020.100007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948131/
https://www.ncbi.nlm.nih.gov/pubmed/33718894
http://dx.doi.org/10.1016/j.xhgg.2020.100007

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