Exome sequencing data analysis to characterize copy number variants involved in m.14487T>C mutation

ABSTRACT: In this study, we analyze DNA whole-exome sequencing (WES) data from 3 patients with m.14487T>C mutation to detect rare candidate SNVs.

ORGANISM(S): Homo sapiens

PROVIDER: GSE131740 | GEO | 2020/05/19

REPOSITORIES: GEO