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2021年1月4日,《核酸研究》(Nucleic Acids Research)在线发表了管敏鑫教授团队有关线粒体tRNA反密码子环37位修饰缺陷导致母系遗传性耳聋的最新研究成果“A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification,processing,stability and aminoacylation of tRNAIle and mitochondrial transla