Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control

The human 22q11.2 chromosomal deletion is one of the strongest identified genetic risk factors for schizophrenia. Although the deletion spans a number of known genes, the contribution of each of these to the 22q11.2 deletion syndrome (DS) is not known. To investigate the effect of individual genes w...

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Detalles Bibliográficos
Autores principales: Maurer, Gianna W., Malita, Alina, Nagy, Stanislav, Koyama, Takashi, Werge, Thomas M., Halberg, Kenneth A., Texada, Michael J., Rewitz, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7205319/
https://www.ncbi.nlm.nih.gov/pubmed/32339168
http://dx.doi.org/10.1371/journal.pgen.1008727

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7205319/
https://www.ncbi.nlm.nih.gov/pubmed/32339168
http://dx.doi.org/10.1371/journal.pgen.1008727

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