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Detection and validation of six pathogenic variants in Chinese inherited heart disease patients using clinical whole-exome sequencing

2021-07-07

Abstract excerpt

The targeted next-generation sequencing (NGS) was employed in detecting the pathogenic mutations in inherited heart disease patients in the present study. Two main methods, the NGS and the classic Sanger sequencing, were used in this study. And, the whole-exome sequencing (WES) was specifically used in this study.

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Literature Corpus work
baba06ae-93be-51fa-affc-77b957f30fc1
DOI
10.22541/au.162566292.28770313/v1
Open publication

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Detection and validation of six pathogenic variants in Chinese inherited heart disease patients using clinical whole-exome sequencingDOI 10.22541/au.162566292.28770313/v1
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