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Association of ERCC1 and XPF polymorphisms with pediatric glioma susceptibility

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摘要 To the Editor:Glioma is a highly invasive and lethal heterogeneous disease caused by glial or precursor cell mutation.It accounts for about 50%of tumors in children and 80%of malignant tumors.[1]The nucleotide excision repair(NER)pathway is a process that involves the sequential assembly of many proteins,including excision repair cross complementation group 1(ERCC1)and xeroderma pigmentosum complementation group F(XPF,also known as ERCC4).
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2023年第6期746-748,共3页 中华医学杂志(英文版)
基金 supported by grants from the National Natural Science Foundation of China(No.81802346) the China Postdoctoral Science Foundation(Nos.2020T130132,2020M682668)
关键词 ERCC1 XPF EXCISION
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