RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism

BACKGROUND: Copy number variants in coding and noncoding genomic regions have been implicated as risk factor for schizophrenia (SCZ). Rare duplications of the RB1CC1 gene were found enriched in SCZ patients. Considering that the effect of such duplications on RB1CC1 expression has never been evaluat...

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Detalles Bibliográficos
Autores principales: Errichiello, Edoardo, Giorda, Roberto, Gambale, Antonella, Iolascon, Achille, Zuffardi, Orsetta, Giglio, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963413/
https://www.ncbi.nlm.nih.gov/pubmed/33340270
http://dx.doi.org/10.1002/mgg3.1561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963413/
https://www.ncbi.nlm.nih.gov/pubmed/33340270
http://dx.doi.org/10.1002/mgg3.1561

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