Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
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DOI: 10.1007/s00439-019-01975-0
Abstract: In this study, we investigated low-frequency and rare variants associated with blood pressure (BP) by focusing on a linkage region on chromosome 16p13. We used whole genome sequencing (WGS) data obtained through the NHLBI Trans-Omics… read more here.
Keywords: blood pressure; evidence; rare variants; associated blood ... See more keywords