Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes

BACKGROUND: Deletions and duplications of the multigenic 16p11.2 and 22q11.2 copy number variant (CNV) regions are associated with brain-related disorders including schizophrenia, intellectual disability, obesity, bipolar disorder, and autism spectrum disorder (ASD). The contribution of individual C...

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Detalles Bibliográficos
Autores principales: Vysotskiy, Mikhail, Zhong, Xue, Miller-Fleming, Tyne W., Zhou, Dan, Cox, Nancy J., Weiss, Lauren A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557010/
https://www.ncbi.nlm.nih.gov/pubmed/34715901
http://dx.doi.org/10.1186/s13073-021-00972-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557010/
https://www.ncbi.nlm.nih.gov/pubmed/34715901
http://dx.doi.org/10.1186/s13073-021-00972-1

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