Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Ahmed ZM; Masmoudi S; Kalay E; Belyantseva IA; Mosrati MA; Collin RW; Riazuddin S; Hmani-Aifa M; Venselaar H; Kawar MN; Tlili A; van der Zwaag B; Khan SY; Ayadi L; Riazuddin SA; Morell RJ; Griffith AJ; Charfedine I; Caylan R; Oostrik J; Karaguzel A; Ghorbel A; Riazuddin S; Friedman TB; Ayadi H; Kremer H; Nature Genetics, 2008, vol. 40, issue 11, p 1335, ISSN 15461718. ISBN 15461718.

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