Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents

Recurrent copy number variations (CNVs) are common causes of neurodevelopmental disorders (NDDs) and associated with a range of psychiatric traits. These CNVs occur at defined genomic regions that are particularly prone to recurrent deletions and duplications and often exhibit variable expressivity...

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Detalles Bibliográficos
Autores principales: Smajlagić, Dinka, Lavrichenko, Ksenia, Berland, Siren, Helgeland, Øyvind, Knudsen, Gun Peggy, Vaudel, Marc, Haavik, Jan, Knappskog, Per Morten, Njølstad, Pål Rasmus, Houge, Gunnar, Johansson, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852900/
https://www.ncbi.nlm.nih.gov/pubmed/32778765
http://dx.doi.org/10.1038/s41431-020-00707-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852900/
https://www.ncbi.nlm.nih.gov/pubmed/32778765
http://dx.doi.org/10.1038/s41431-020-00707-7

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