Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
- Cited forNUCLEOTIDE SEQUENCE [MRNA], SUBCELLULAR LOCATION, TISSUE SPECIFICITY, DEVELOPMENTAL STAGE
- Strain
- TissueBrain
- CategoriesSequences, Expression, Subcellular Location
- SourceUniProtKB reviewed (Swiss-Prot)