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Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling

SHANK3 deficiency represents one of the most replicated monogenic risk factors for autism spectrum disorder (ASD) and SHANK3 caused ASD presents a unique opportunity to understand the underlying neuropathological mechanisms of ASD. In this study, genetic tests, comprehensive clinical and neurobehavi...

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Detalles Bibliográficos
Autores principales:	Liu, Chunxue, Li, Dongyun, Yang, Haowei, Li, Huiping, Xu, Qiong, Zhou, Bingrui, Hu, Chunchun, Li, Chunyang, Wang, Yi, Qiao, Zhongwei, Jiang, Yong-hui, Xu, Xiu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572121/ https://www.ncbi.nlm.nih.gov/pubmed/33388374 http://dx.doi.org/10.1016/j.pneurobio.2020.101985

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William Frederick Shanks
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