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Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
Ji, Yanchun; Zhang, Juanjuan; Yu, Jialing; Wang, Ying; Lu, Yuanyuan; Liang, Min; Li, Qiang; Jin, Xiaofen; Wei, Yinsheng; Meng, Feilong; Gao, Yinglong; Cang, Xiaohui; Tong, Yi; Liu, Xiaoling; Zhang, Minglian; Jiang, Peifang; Zhu, Tao; Mo, Jun Qin; Huang, Taosheng; Jiang, Pingping; Guan, Min-Xin.
Affiliation
  • Ji Y; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Zhang J; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Yu J; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Wang Y; School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Lu Y; Attardi Institute of Mitochondrial Biomedicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Liang M; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Li Q; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Jin X; Department of Ophthalmology, Chinese Academy of Traditional Chinese Medicine, Beijing, China.
  • Wei Y; School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Meng F; Attardi Institute of Mitochondrial Biomedicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Gao Y; Attardi Institute of Mitochondrial Biomedicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Cang X; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Tong Y; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Liu X; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Zhang M; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Jiang P; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Zhu T; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Mo JQ; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Huang T; Division of Medical Genetics and Genomics, the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Jiang P; Institute of Genetics, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • Guan MX; School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Hum Mol Genet ; 28(9): 1515-1529, 2019 05 01.
Article in En | MEDLINE | ID: mdl-30597069
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Optic Atrophy, Hereditary, Leber / Alleles / Mitochondria / Mutation / NADH Dehydrogenase Type of study: Prognostic_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Optic Atrophy, Hereditary, Leber / Alleles / Mitochondria / Mutation / NADH Dehydrogenase Type of study: Prognostic_studies Limits: Animals Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2019 Document type: Article Affiliation country: Country of publication: