Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders

22q11.2 deletion syndrome (22q11.2DS) is a disorder caused by the segmental deletion of human chromosome 22. This chromosomal deletion is known as high genetic risk factors for various psychiatric disorders. The different deletion types are identified in 22q11.2DS patients, including the most common...

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Detalhes bibliográficos
Publicado no:Mol Brain
Main Authors: Saito, Ryo, Miyoshi, Chika, Koebis, Michinori, Kushima, Itaru, Nakao, Kazuki, Mori, Daisuke, Ozaki, Norio, Funato, Hiromasa, Yanagisawa, Masashi, Aiba, Atsu
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8042712/
https://ncbi.nlm.nih.gov/pubmed/33845872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-021-00778-7
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