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

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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3337078/
https://ncbi.nlm.nih.gov/pubmed/22832905
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/tp.2012.31
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