1. C Modulation of anril expression may mediate the association between chromosome 9p21 variants and coronary atherosclerosis risk. (22nd September 2015) Authors: Cunnington, M S; Santibanez Koref, M; Mayosi, B; Burn, J; Keavney, B Journal: Heart Issue: Volume 96(2010)Supplement 1 Page Start: A2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. FRI0379 Prevalence of FAM111 B gene mutations in systemic sclerosis. (15th June 2017) Authors: Gcelu, A; Deshpande, G; Kalla, AA; Tikly, M; Mayosi, B; Hodkinson, B Journal: Annals of the rheumatic diseases Issue: Volume 76(2017)Supplement 2 Page Start: 631 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy. Issue 3 (March 1998) Authors: Moolman-Smook, J C; Mayosi, B; Brink, P; Corfield, V A Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 253 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗