Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans
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author: Robert J. Morell, Hanka Venselaar, Abdelaziz Tlili, Inna A Belyantseva, Thomas B. Friedman, Hannie Kremer, Saima Riazuddin, Sheikh Riazuddin, Rob W J Collin, Ersan Kalay, Bert van der Zwaag, Jaap Oostrik, Refik Caylan, Ahmet Karagüzel, S Amer Riazuddin, Saber Masmoudi
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