Expression of Genes in the 16p11.2 Locus during Development of the Human Fetal Cerebral Cortex

The 593 kbp 16p11.2 copy number variation (CNV) affects the gene dosage of 29 protein coding genes, with heterozygous 16p11.2 microduplication or microdeletion implicated in about 1% of autism spectrum disorder (ASD) cases. The 16p11.2 CNV is frequently associated with macrocephaly or microcephaly i...

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Detalles Bibliográficos
Autores principales: Morson, Sarah, Yang, Yifei, Price, David J, Pratt, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328201/
https://www.ncbi.nlm.nih.gov/pubmed/33825894
http://dx.doi.org/10.1093/cercor/bhab067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328201/
https://www.ncbi.nlm.nih.gov/pubmed/33825894
http://dx.doi.org/10.1093/cercor/bhab067

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