Author:
Guha Sanjukta,Chaurasia Sunita,Ramachandran Charanya,Roy Sanhita
Publisher
Springer Science and Business Media LLC
Reference53 articles.
1. Kirkness, C. M., McCartney, A., Rice, N. S., Garner, A. & Steele, A. D. Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology. Br J Ophthalmol 71, 130–144 (1987).
2. Vithana, E. N. et al. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat Genet 38, 755–757 (2006).
3. Vithana, E. N. et al. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum Mol Genet 17, 656–666 (2008).
4. Sultana, A., Garg, P., Ramamurthy, B., Vemuganti, G. K. & Kannabiran, C. Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy. Mol Vis 13, 1327–1332 (2007).
5. Park, M., Li, Q., Shcheynikov, N., Zeng, W. & Muallem, S. NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation. Mol Cell 16, 331–341 (2004).
Cited by
44 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献