Two novel heterozygous truncating variants in <i>NR4A2</i> identified in patients with neurodevelopmental disorder and brief literature review.

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作者： Xiaozhen,Song ^[1] ; Wuhen,Xu ^[1] ; Man,Xiao ^[1] ; Yanfen,Lu ^[2] ; Xiaoping,Lan ^[1] ; Xiaojun,Tang ^[1] ; Nanjie,Xu ^[3] ; Guangjun,Yu ^[4] ; Hong,Zhang ^[5] ; Shengnan,Wu ^[1]

作者单位： Molecular Diagnostic Laboratory, Department of Clinical Laboratory, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. ^[1] Department of Neurology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. ^[2] Research Center of Translational Medicine, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. ^[3] Department of Anatomy and Physiology, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. ^[4] Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. ^[5]

关键词 NR4A2 attention deficit intellectual disability language impairment neurodevelopmental disorder truncating

DOI 10.3389/fnins.2022.956429

PMID 35992907

发布时间 2022-08-23

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Frontiers in neuroscience

2022年16卷

956429页

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Two novel heterozygous truncating variants in <i>NR4A2</i> identified in patients with neurodevelopmental disorder and brief literature review.

Frontiers in neuroscience

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Frontiers in neuroscience

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Two novel heterozygous truncating variants in <i>NR4A2</i> identified in patients with neurodevelopmental disorder and brief literature review.

Frontiers in neuroscience

相似文献

Frontiers in neuroscience

相关期刊

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