Mouse Models of 22q11.2-Associated Autism Spectrum Disorder

Copy number variation (CNV) of human chromosome 22q11.2 is associated with an elevated rate of autism spectrum disorder (ASD) and represents one of syndromic ASDs with rare genetic variants. However, the precise genetic basis of this association remains unclear due to its relatively large hemizygous...

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Detalles Bibliográficos
Autores principales: Hiroi, Noboru, Hiramoto, Takeshi, Harper, Kathryn M., Suzuki, Go, Boku, Shuken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118685/
https://www.ncbi.nlm.nih.gov/pubmed/25089229
http://dx.doi.org/10.4172/2165-7890.S1-001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118685/
https://www.ncbi.nlm.nih.gov/pubmed/25089229
http://dx.doi.org/10.4172/2165-7890.S1-001

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