1. A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss. Issue 5 (1st May 2000) Authors: Morlé, Laurette; Bozon, Muriel; Alloisio, Nicole; Latour, Philippe; Vandenberghe, Antoon; Plauchu, Henri; Collet, Lionel; Edery, Patrick; Godet, Jacqueline; Lina-Granade, Geneviève Journal: Journal of medical genetics Issue: Volume 37:Issue 5(2000) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗