Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees-Reference-Cited by-同舟云学术

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Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees

Published:2017-10-05 Issue:6 Volume:16 Page:8997-9004
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Ji Yanchun,Qiao Lihua,Liang Xiaoyang,Zhu Ling,Gao Yinglong,Zhang Juanjuan,Jia Zidong,Wei Qi-Ping,Liu Xiaoling,Jiang Pingping,Guan Min-Xin

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel mitochondrial tRNALeu(UUR) 3261A > g mutation in two pedigrees with essential hypertension;Irish Journal of Medical Science (1971 -);2022-06-03

2. Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families;World Journal of Clinical Cases;2022-01-07

3. Maternally transmitted diabetes mellitus may be associated with mitochondrial ND5 T12338C and tRNAAla T5587C variants;Irish Journal of Medical Science (1971 -);2022-01-06

4. Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia;Human Heredity;2022

5. Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus;International Journal of General Medicine;2021-09

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