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

• Main Authors: Vithana, E.N., Tan, D.T.H., Yong, V.H.K., 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., Khine, M., Salto-Tellez, M., Guo, K., Aung Tin
• 其他作者: OPHTHALMOLOGY
• 格式: Article
• 出版: 2012
• 在線閱讀: http://scholarbank.nus.edu.sg/handle/10635/33171

10.1038/ng1824