Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome

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Chromosome 22q11.2 deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans. It is typified by highly variable symptoms, which might be explained by epigenetic regulation of genes in the interval. Using computational algorithms, our laboratory previously predicted that DiGeorg...

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Detalles Bibliográficos
Autores principales: Chakraborty, D, Bernal, A J, Schoch, K, Howard, T D, Ip, E H, Hooper, S R, Keshavan, M S, Jirtle, R L, Shashi, V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337078/
https://www.ncbi.nlm.nih.gov/pubmed/22832905
http://dx.doi.org/10.1038/tp.2012.31

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337078/
https://www.ncbi.nlm.nih.gov/pubmed/22832905
http://dx.doi.org/10.1038/tp.2012.31

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