CHD2 variants
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下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP361006
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资源简介：
Three CHD2 variants identified in Chinese children
应用场景：
创建时间：
2026-02-21
相关数据集
Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders
Project description De novo pathogenic variants in CHD2 are one of the most common causes of the neurodevelopmental disorders (NDDs) that include refractory epilepsy, intellectual disability and autis
Zenodo2026-01-16 更新00
Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders [RNA-seq]
De novo pathogenic variants in CHD2 are one of the most common causes of the neurodevelopmental disorders (NDDs) that include refractory epilepsy, intellectual disability and autism spectrum disorders
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CHD2 Regulates Neuron-glioma Interactions in Pediatric Glioma
High-grade gliomas (HGG) are deadly diseases for both adult and pediatric patients. Recently, it has been shown that neuronal activity promotes the progression of multiple subgroups of HGG. However, e
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Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders
Project description De novo pathogenic variants in CHD2 are one of the most common causes of the neurodevelopmental disorders (NDDs) that include refractory epilepsy, intellectual disability and autis
Zenodo2026-01-16 更新00
CHD2 Regulates Neuron-glioma Interactions in Pediatric Glioma. CHD2 Regulates Neuron-glioma Interactions in Pediatric Glioma
High-grade gliomas (HGG) are deadly diseases for both adult and pediatric patients. Recently, it has been shown that neuronal activity promotes the progression of multiple subgroups of HGG. However, e
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