Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
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Date
Authors
Ahmed, Z.M.
Masmoudi, S.
Kalay, E. Ersan
Belyantseva, I.A.
Mosrati, M.A.
Collin, R.W.J. Rob
Hmani-Aifa, M.
Venselaar, H. Hanka
Kawar, M.N.
Tlili, A.
