1. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. Issue 1 (6th July 2006) Authors: Jiao, Xiaodong; Sultana, Afia; Garg, Prashant; Ramamurthy, Balasubramanya; Vemuganti, Geeta K; Gangopadhyay, Nibaran; Hejtmancik, J Fielding; Kannabiran, Chitra Journal: Journal of medical genetics Issue: Volume 44:Issue 1(2007) Page Start: 64 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Impaired AMPA receptor trafficking by a double knockout of zebrafish olfactomedin1a/b. Issue 6 (6th November 2017) Authors: Nakaya, Naoki; Sultana, Afia; Tomarev, Stanislav I. Journal: Journal of neurochemistry Issue: Volume 143:Issue 6(2017) Page Start: 635 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗