1. Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the γ chain globular domain impairing fibrinogen secretion. Issue 9 (1st September 2005) Authors: Vu, D; de Moerloose, P; Batorova, A; Lazur, J; Palumbo, L; Neerman-Arbez, M Journal: Journal of medical genetics Issue: Volume 42:Issue 9(2005) Page Start: e57 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗