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

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 morphology; h...

Descripción completa

Detalles Bibliográficos
Autores principales: Jonsson, Lina, Martin, Joanna, Lichtenstein, Paul, Magnusson, Patrik K. E., Lundström, Sebastian, Westberg, Lars, Tammimies, Kristiina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422071/
https://www.ncbi.nlm.nih.gov/pubmed/37156729
http://dx.doi.org/10.1002/mgg3.2191

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422071/
https://www.ncbi.nlm.nih.gov/pubmed/37156729
http://dx.doi.org/10.1002/mgg3.2191

Ejemplares similares