1. 6C.01: CULLIN-3 MUTATIONS LEADING TO SKIPPING OF EXON 9 ARE RESPONSIBLE FOR SEVERE CASES OF FAMILIAL HYPERKALAEMIC HYPERTENSION. (June 2015) Authors: Picard, H. Louis Dit; Latreche, S.; Thurairajasingam, N.; Auzan, C.; Fiquet, B.; Frayssinet, R.; Garnier, A.; Jendruchova, V.; Lobbedez, T.; Martorell, L.; Mortier, G.; Pela, I.; Taque, S.; Vargas-Poussou, R.; Clauser, E.; Jeunemaitre, X. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗