Kumar, G. S., Kyle, J. W., Minogue, P. J., Kumar, K. D., Vasantha, K., Berthoud, V. M., . . . Sathiyavedu, S. T. (2012). An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract.

Kumar, G. Senthil, John W. Kyle, Peter J. Minogue, K. Dinesh Kumar, K. Vasantha, Viviana M. Berthoud, Eric C. Beyer, và Santhiya T. Sathiyavedu. An MIP/AQP0 Mutation With Impaired Trafficking and Function Underlies an Autosomal Dominant Congenital Lamellar Cataract. 2012.

Kumar, G. Senthil, et al. An MIP/AQP0 Mutation With Impaired Trafficking and Function Underlies an Autosomal Dominant Congenital Lamellar Cataract. 2012.