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Original research
Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia

Authors

  1. Correspondence to Prof David Curtis, UCL Genetics Institute, University College London, London WC1E 6BT, UK; d.curtis{at}ucl.ac.uk
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Citation

Curtis D
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.

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