1. Missense mutations in the perforin (PRF1) gene as a cause of hereditary cancer predisposition. (2nd July 2016) Authors: Chaudhry, Mohammed S.; Gilmour, Kimberly C.; House, Imran G.; Layton, Mark; Panoskaltsis, Nicki; Sohal, Mamta; Trapani, Joseph A.; Voskoboinik, Ilia Journal: Oncoimmunology Issue: Volume 5:Number 7(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗