Examining neurodevelopmental problems in 15q11.2 (BP1‐BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample

Examining neurodevelopmental problems in 15q11.2 (BP1‐BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample

Abstract Background Several copy number variations (CNVs) are associated with increased risk for neurodevelopmental and psychiatric disorders. The CNV 15q11.2 (BP1‐BP2) deletion has been associated with learning difficulties, attention deficit hyperactivity disorder (ADHD), epilepsy, and brain morph...

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Bibliographic Details
Main Authors: Lina Jonsson, Joanna Martin, Paul Lichtenstein, Patrik K. E. Magnusson, Sebastian Lundström, Lars Westberg, Kristiina Tammimies
Format: Article
Language:English
Published: Wiley 2023-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
15q11.2
DNA copy number variations
neurodevelopmental disorders
Online Access:https://doi.org/10.1002/mgg3.2191

Internet

https://doi.org/10.1002/mgg3.2191

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