Mhaske, P. V., Levit, N. A., Li, L., Wang, H., Lee, J. R., Shuja, Z., . . . White, T. W. (2013). The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity. American Physiological Society.

Mhaske, Pallavi V., Noah A. Levit, Leping Li, Hong-Zhan Wang, Jack R. Lee, Zunaira Shuja, Peter R. Brink, i Thomas W. White. The Human Cx26-D50A and Cx26-A88V Mutations Causing Keratitis-ichthyosis-deafness Syndrome Display Increased Hemichannel Activity. American Physiological Society, 2013.

Mhaske, Pallavi V., et al. The Human Cx26-D50A and Cx26-A88V Mutations Causing Keratitis-ichthyosis-deafness Syndrome Display Increased Hemichannel Activity. American Physiological Society, 2013.