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Dive into the research topics of 'Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease'. Together they form a unique fingerprint.- Sort by
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Yohei Kirino, Takehiro Yasukawa, Shigeo Ohta, Shigeo Akira, Kaisuke Ishihara, Kimitsuna Watanabe, Tsutomu Suzuki
Research output: Contribution to journal › Article › peer-review