Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene

by Mehta, J.S., Tan, D.T., Aung, T., Vithana, E.N., Hemadevi, B., Sundaresan, P., Arunkumar, J., Srinivasan, M., Prajna, V.
Published 2011

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

by 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
Published 2012