Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
暂无分享,去创建一个
B. van der Zwaag | H. Kremer | S. Riazuddin | Z. Ahmed | S. Riazuddin | A. Griffith | T. Friedman | H. Venselaar | S. Y. Khan | Mohamed Ali Mosrati | A. Tlili | S. Masmoudi | R. Collin | H. Ayadi | E. Kalay | B. Zwaag | R. Morell | Zubair M. Ahmed | I. Belyantseva | J. Oostrik | A. Ghorbel | R. Çaylan | S. Riazuddin | Leila Ayadi | A. Karaguzel | M. Hmani-Aifa | A. Karagüzel | I. Charfedine | Mayya N Kawar | Tlili Abdelaziz | Mounira Hmani-Aifa | Hannie Kremer