We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.AuthorsAhmed 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 HPublicationNature genetics, 2008, Vol 40, Issue 11, p1335ISSN1546-1718Publication typearticleDOI10.1038/ng.245