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Whole Exome Sequencing for Identification of Pathogenic Variants in Hypertrophic Cardiomyopathy Egyptian patients

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NIAID Data Ecosystem2026-05-10 收录
下载链接:
https://www.ncbi.nlm.nih.gov/sra/SRP478439
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The major goal of this study is to detect genetic variants which useful to specify sudden cardiac death risk in hypertrophic cardiomyopathy predisposed individuals by stratifying them into different risk categories, thus furnishing crucial information to facilitate pre-symptomatic diagnosis and implementation of primary prevention strategies in high-risk individuals, and decreasing the mortality rate.
创建时间:
2025-10-01
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