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Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss.
Zheng, Jing; Bai, Xiaohui; Xiao, Yun; Ji, Yanchun; Meng, Feilong; Aishanjiang, Maerhaba; Gao, Yinglong; Wang, Haibo; Fu, Yong; Guan, Min-Xin.
Afiliación
  • Zheng J; 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; Institute of Genetics, Zhejiang University School of Med
  • Bai X; Department of Otorhinolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, Shandong 250022, China.
  • Xiao Y; 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; Department of Otorhinolaryngology-Head and Neck Surgery,
  • Ji Y; 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; Institute of Genetics, Zhejiang University School of Med
  • Meng F; 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; Institute of Genetics, Zhejiang University School of Med
  • Aishanjiang M; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310058, China.
  • Gao Y; 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; Institute of Genetics, Zhejiang University School of Med
  • Wang H; Department of Otorhinolaryngology-Head and Neck Surgery, Shandong Provincial ENT Hospital, Shandong University, Jinan, Shandong 250022, China. Electronic address: whboto11@email.sdu.edu.cn.
  • Fu Y; 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; Department of Otorhinolaryngology Head and Neck Surgery,
  • Guan MX; 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; Institute of Genetics, Zhejiang University School of Med
Mitochondrion ; 52: 163-172, 2020 05.
Article en En | MEDLINE | ID: mdl-32169613
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN de Transferencia / Análisis de Secuencia de ADN / Pueblo Asiatico / Pérdida Auditiva / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mitochondrion Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN de Transferencia / Análisis de Secuencia de ADN / Pueblo Asiatico / Pérdida Auditiva / Mutación Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mitochondrion Año: 2020 Tipo del documento: Article