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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Detalles Bibliográficos
Autores principales: Saito, Ryo, Miyoshi, Chika, Koebis, Michinori, Kushima, Itaru, Nakao, Kazuki, Mori, Daisuke, Ozaki, Norio, Funato, Hiromasa, Yanagisawa, Masashi, Aiba, Atsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042712/
https://www.ncbi.nlm.nih.gov/pubmed/33845872
http://dx.doi.org/10.1186/s13041-021-00778-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042712/
https://www.ncbi.nlm.nih.gov/pubmed/33845872
http://dx.doi.org/10.1186/s13041-021-00778-7

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