Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature

Copy number variants (CNVs) play an important role in the genetic underpinnings of neuropsychiatric/neurodevelopmental disorders. The chromosomal region 16p11.2 (BP4–BP5) harbours both deletions and duplications that are associated in carriers with neurodevelopmental and neuropsychiatric conditions...

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Detalhes bibliográficos
Publicado no:Int J Environ Res Public Health
Main Authors: Oliva-Teles, Natália, de Stefano, Maria Chiara, Gallagher, Louise, Rakic, Severin, Jorge, Paula, Cuturilo, Goran, Markovska-Simoska, Silvana, Borg, Isabella, Wolstencroft, Jeanne, Tümer, Zeynep, Harwood, Adrian J., Kodra, Yllka, Skuse, David
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Review
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7763014/
https://ncbi.nlm.nih.gov/pubmed/33321999
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijerph17249253
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