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APA Citation
Martin, R., Latten, M., Hart, P., Murray, H., Bailie, D. A., Crockard, M., Lamont, J., Fitzgerald, P., & Graham, C. A. (2016). genetic diagnosis of familial hypercholesterolaemia using a rapid biochip array assay for 40 common LDLR, APOB and PCSK9 mutations. Atherosclerosis, 254, 8–13. http://access.bl.uk/ark:/81055/vdc_100039991832.0x00005b