Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics

22q11.2 deletion syndrome (22q11DS) results from a hemizygous deletion that typically spans 46 protein-coding genes and is associated with widespread alterations in brain morphology. The specific genetic mechanisms underlying these alterations remain unclear. In the 22q11.2 ENIGMA Working Group, we...

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Detalles Bibliográficos
Autores principales: Forsyth, Jennifer K, Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R K, Villalon-Reina, Julio E, Thompson, Paul M, Bearden, Carrie E
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/PMC8196250/
https://www.ncbi.nlm.nih.gov/pubmed/33638978
http://dx.doi.org/10.1093/cercor/bhab008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196250/
https://www.ncbi.nlm.nih.gov/pubmed/33638978
http://dx.doi.org/10.1093/cercor/bhab008

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