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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763014/
https://www.ncbi.nlm.nih.gov/pubmed/33321999
http://dx.doi.org/10.3390/ijerph17249253

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763014/
https://www.ncbi.nlm.nih.gov/pubmed/33321999
http://dx.doi.org/10.3390/ijerph17249253

Ejemplares similares