Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

• Main Authors: Vithana, E.N., Tan, D.T.H., Venkataraman, D., Yong, V.H.K., Aung, T., Morgan, P., Casey, J.R., Sundaresan, P., Hemadevi, B., Srinivasan, M., Prajna, V., Ebenezer, N.D., Mohamed, M.D., Inglehearn, C.F., Anand, S., Khine, K.O., Salto-Tellez, M., Guo, K.
• Other Authors: OPHTHALMOLOGY
• Format: Article
• Published: 2011
• Online Access: http://scholarbank.nus.edu.sg/handle/10635/26618
• Institution: National University of Singapore

Nature Genetics