QuickView for TRMT10C;jsessionid=48F476EEDA5C0C6C45D14ECEB383885F (gene)

1. The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria.
2. Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired …
3. Reduction of Drosophila Mitochondrial RNase P in Skeletal and Heart Muscle Causes Muscle Degeneratio…
4. Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respirator…
5. Disease-associated mutations in mitochondrial precursor tRNAs affect binding, m1R9 methylation, and …

There were no clinical trials for TRMT10C;jsessionid=48F476EEDA5C0C6C45D14ECEB383885F