Exome sequencing data analysis to characterize copy number variants involved in m.14487T>C mutation
收藏NIAID Data Ecosystem2026-03-11 收录
下载链接：
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131740
下载链接
链接失效反馈官方服务：
资源简介：
In this study, we analyze DNA whole-exome sequencing (WES) data from 3 patients with m.14487T>C mutation to detect rare candidate SNVs. Examination of EDTA blood of each patient or their biological parents (trio) with m.14487T>C mutation by deep sequencing
创建时间：
2020-05-19
