摘要 : Mitochondrial 12S rRNA 1555A>G mutation is one of the important causes of aminoglycoside-induced and nonsyndromic deafness. Our previous investigations showed that the A1555G mutation was a primary factor underlying the developmen... 展开
作者 | Zhu~ Yi Yang~ Li Tang~ Xiaowen Chen~ Bobei Ding~ Yu Li~ Yongyan You~ Junyan Zheng~ Jing Tao~ Zhihua Zhao~ Fuxin Wang~ Jindan Sun~ Dongmei Zhao~ Jianyue Meng~ Yanzi Guan~ Min-Xin Lu~ Jianxin Qian~ Yaping Li~ Zhiyuan Yang~ Aifen Li~ Ronghua |
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作者单位 | |
期刊名称 | 《Mitochondrion》 |
总页数 | 13 |
语种/中图分类号 | 英语 / Q93 |
关键词 | mitochondrial haplotype phenotypic manifestation |
馆藏号 | N2008EPST0011265 |