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Dive into the research topics of 'Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans'. Together they form a unique fingerprint.- Sort by
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Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay, Inna A. Belyantseva, Mohamed Ali Mosrati, Rob W.J. Collin, Saima Riazuddin, Mounira Hmani-Aifa, Hanka Venselaar, Mayya N. Kawar, Abdelaziz Tlili, Bert van der Zwaag, Shahid Y. Khan, Leila Ayadi, S. Amer Riazuddin, Robert J. Morell, Andrew J. Griffith, Ilhem Charfedine, Refik Ҫaylan, Jaap Oostrik
Research output: Contribution to journal › Article › peer-review