Associated Papers
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.
Charif M et al.
Molecular Biology Reports, 2012
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Ahmed ZM et al.
Nature Genetics, 2008
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