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Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with high phenotypic and genetic heterogeneity. Whole-exome sequencing studies have shown that de novo single-nucleotide variations (SNVs) play an important role in sporadic ASD. The present study aimed to search for de novo SNVs using...
Autores principales: | Jiao, Jian, Zhang, Manxue, Yang, Pingyuan, Huang, Yan, Hu, Xiao, Cai, Jia, Yang, Chan, Situ, Mingjing, Zhang, Hui, Fu, Lei, Guo, Kuifang, Huang, Yi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018782/ https://www.ncbi.nlm.nih.gov/pubmed/31838722 http://dx.doi.org/10.1007/s12031-019-01456-z |
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