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