Whole-genome sequencing identified novel mutations in a Chinese family with lynch syndrome.

Wan He,Shaowei Dong,Jing Shen, Jiutong Wu,Pan Zhao,Dongbing Li,Dongliang Wang,Na Tang,Chang Zou

Frontiers in oncology（2023）

引用 1|浏览3

暂无评分

摘要

Our findings extend the mutation spectrum of genes associated with LS in MLH2 and FSHR, which is essential for future screening and genetic diagnosis of LS.

查看译文

关键词

FSHR,Lynch syndrome,MMR pathway,MSH2,whole genome sequencing

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要