Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy.

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第一作者： Zhiying,Xie

第一单位： Department of Neurology, Peking University First Hospital, Beijing, China.

作者： Zhiying,Xie ^[1] ; Chang,Liu ^[1] ; Yanyu,Lu ^[1] ; Chengyue,Sun ^[2] ; Yilin,Liu ^[3] ; Meng,Yu ^[1] ; Junlong,Shu ^[1] ; Lingchao,Meng ^[1] ; Jianwen,Deng ^[1] ; Wei,Zhang ^[1] ; Zhaoxia,Wang ^[1] ; He,Lv ^[1] ; Yun,Yuan ^[1]

作者单位： Department of Neurology, Peking University First Hospital, Beijing, China. ^[1] Department of Neurology, Peking University People's Hospital, Beijing, China. ^[2] Department of Pathology, Peking Union Medical College Hospital, Beijing, China. ^[3]

关键词 DMD LINE-1 aberrant splicing deep-intronic structural variant long-read sequencing

DOI 10.3389/fgene.2022.979732

PMID 36092865

发布时间 2022-09-13

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Frontiers in genetics

2022年13卷

979732页

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Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy.

Frontiers in genetics

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Frontiers in genetics

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Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy.

Frontiers in genetics

相似文献

Frontiers in genetics

相关期刊

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