Additional file 9 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile

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Figshare2021-08-12 更新2026-04-08 收录

儿科遗传病

DNA甲基化分析

数据链接：

https://springernature.figshare.com/articles/dataset/Additional_file_9_of_Childhood-onset_dystonia-causing_KMT2B_variants_result_in_a_distinctive_genomic_hypermethylation_profile/15153913/1 数据链接链接失效反馈

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资源简介：

Additional file 9: Table S1. Clinical characterization of the study cohort.

提供机构：

Prontera, Paolo; Pizzi, Simone; Niceta, Marcello; Pedace, Lucia; Capuano, Alessandro; Reale, Chiara; Ciolfi, Andrea; Agolini, Emanuele; Olson, Rory J.; Gavrilova, Ralitza H.; Sadikovic, Bekim; Bedeschi, Maria Francesca; Andreani, Marco; Iascone, Maria; Soliveri, Paola; Schultz-Rogers, Laura; Zorzi, Giovanna S.; Galosi, Serena; Travaglini, Lorena; Tartaglia, Marco; Leuzzi, Vincenzo; Garibaldi, Matteo; Foroutan, Aidin; Panteghini, Celeste; Miele, Evelina; Garavaglia, Barbara M.; Invernizzi, Federica

创建时间：

2021-08-12

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