Browsing by Author Bay, Veysel
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) |
|---|---|---|
| Feb-2016 | Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations | Aypek, Hande; Bay, Veysel; Meşe, Gülistan |
| Jun-2013 | Characterization of connexin 26 mutations causing hereditary skin disorders | Bay, Veysel |