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DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modification
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Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease Yohei Kirino, Takehiro Yasukawa, Shigeo Ohta, Proceedings of the National Academy of Sciences Mitochondrial MyopathyMt TrnaMitochondrial FunctionMitochondrial BiogenesisMedicine | 2004 | 284 |
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