Additional file 10 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile
This dataset is Additional File 10 (Table S2) from the research paper titled 'Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile'. It contains the sex and age information of patient and control groups used in the episignature discovery analysis. The data is derived from individual samples in clinical studies and aims to support research on epigenetic markers associated with KMT2B variant-related hereditary dystonia, providing foundational data for exploring disease mechanisms and identifying potential biomarkers.
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About
This dataset is Additional File 10 (Table S2) from the research paper titled 'Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile'. It contains the sex and age information of patient and control groups used in the episignature discovery analysis. The data is derived from individual samples in clinical studies and aims to support research on epigenetic markers associated with KMT2B variant-related hereditary dystonia, providing foundational data for exploring disease mechanisms and identifying potential biomarkers.
https://springernature.figshare.com/articles/dataset/Additional_file_10_of_Childhood-onset_dystonia-causing_KMT2B_variants_result_in_a_distinctive_genomic_hypermethylation_profile/15153874
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数据说明
该数据集是研究论文《儿童期发病性肌张力障碍相关KMT2B基因变异导致独特的基因组高甲基化特征》的补充文件10，具体为表S2。它包含用于表观遗传特征（episignature）发现分析的患者组和对照组的性别与年龄信息，数据来源于临床研究中的个体样本，旨在支持KMT2B基因变异相关遗传性肌张力障碍的表观遗传标记研究，为疾病机制探索和潜在生物标志物识别提供基础数据。
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