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LRTOMT: a new tone in understanding the symphony of non-syndromic deafness |
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| Authors: | JM Schulze |
| Affiliation: | Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, 950 West 28th Avenue, Vancouver, BC, Canada V5Z 4H4. e-mail: |
| Abstract: | Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans Ahmed et al. (2008) Nature Genetics 40: 1335–1340. |
| Keywords: | |