m.7472insC, MT-TS1, Hearing loss with neurological dysfunction / ataxia / myoclonus
| tRNA variant | m.7472insC |
| Gene | MT-TS1 |
| Disease | Hearing loss with neurological dysfunction / ataxia / myoclonus |
| Description | Alters tRNA structure and processing. |
| tRNAs | trbR00001085 |
| Publications |
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