1. Clinical features and possible founder mutation of the 8bp duplication mutation in the SLC4A11 gene causing corneal dystrophy and perceptive deafness in three South American families. (4th March 2019) Authors: Romero, Pablo T.; Donoso, Rodrigo; López, Pamela; Miranda, Ana; Rodríguez, Leandro; Chrzanowsky, Dominique; Asenjo, Maria S.; Burgos, Gonzalo; Villegas, Pablo; Desir, Julie; Moya, Graciela; Herrera, Luisa M. Journal: Ophthalmic genetics Issue: Volume 40:Number 2(2019) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗