Article info
PDFGenome-wide studies
Original research
Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia
- Correspondence to Prof David Curtis, UCL Genetics Institute, University College London, London WC1E 6BT, UK; d.curtis{at}ucl.ac.uk
Citation
Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia
Publication history
- Received January 26, 2021
- Revised March 18, 2021
- Accepted April 15, 2021
- First published April 28, 2021.
Online issue publication
November 15, 2022
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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.