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J-GLOBAL ID：202002210474468154   整理番号：20A1092447

難聴の中国人被検者887人におけるミトコンドリアtRNA突然変異

Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss

著者 (17件)： Zheng Jing (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Zheng Jing (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China) ,  Bai Xiaohui (Department of Otorhinolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, Shandong 250022, China) ,  Xiao Yun (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Xiao Yun (Department of Otorhinolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, Shandong 250022, China) ,  Ji Yanchun (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Ji Yanchun (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China) ,  Meng Feilong (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Meng Feilong (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China) ,  Aishanjiang Maerhaba (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China) ,  Gao Yinglong (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Gao Yinglong (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China) ,  Wang Haibo (Department of Otorhinolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, Shandong 250022, China) ,  Fu Yong (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Fu Yong (Department of Otorhinolaryngology Head and Neck Surgery, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Guan Min-Xin (Division of Medical Genetics and Genomics, and Department of Genetic and Metabolic Diseases, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang 310052, China) ,  Guan Min-Xin (Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China)
資料名： Mitochondrion  (Mitochondrion)
巻： 52  ページ： 163-172  発行年： 2020年05月 
JST資料番号： W1366A  ISSN： 1567-7249  資料種別： 逐次刊行物 (A)
記事区分： 原著論文  発行国： オランダ (NLD)  言語： 英語 (EN)

抄録/ポイント： ミトコンドリアtRNAの変異は難聴の重要な原因であることが報...

シソーラス用語： ヒト ,...
準シソーラス用語： *ミトコンドリアtRNA ,...

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著者キーワード (5件)： 聴力損失 ,  tRNA変異体 ,  有病率 ,  ミトコンドリア ,  中国

分類 (5件)： 細胞構成体一般  (EF03010Z) ,  遺伝的変異  (EC01030Y) ,  先天性疾患・奇形一般  (GD03010V) ,  耳鼻咽喉科の臨床医学一般  (GQ01030Q) ,  疫学  (GB03000E)

タイトルに関連する用語 (6件)： 難聴 ,  中国人 ,  被検者 ,  ミトコンドリア ,  tRNA ,  突然変異