Cite
HARVARD Citation
Curtis, D. (2022). Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia. Journal of medical genetics. 59 (6), pp. 597-604. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Curtis, D. (2022). Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia. Journal of medical genetics. 59 (6), pp. 597-604. [Online].