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Acute Respiratory Failure Is the Initial Manifestation in the Adult-Onset A3243G tRNALeu mtDNA Mutation: A Case Report and the Literature Review 期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:  Pan, Xiaoli;  Wang, Lijun;  Fei, Guoqiang;  Dong, Jihong;  Zhong, Chunjiu
收藏  |  浏览/下载:37/0  |  提交时间:2019/12/05
Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation 期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
作者:  Wang, Wei;  Zhuang, Qianqian;  Ji, Kunqian;  Wen, Bing;  Lin, Pengfei
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/12
Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap 期刊论文
NEUROLOGY INDIA, 2016, 卷号: 64, 期号: 2, 页码: 336-U208
作者:  Liu, Fuchen;  Zhang, Dong;  Yan, Chuanzhu
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/17
Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes 期刊论文
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 卷号: 8, 期号: 6, 页码: 7022-7027
作者:  Li, Weiwei;  Zhang, Wei;  Li, Fang;  Wang, Cailing
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/17
Leigh综合征及两种肿瘤的分子遗传学研究 学位论文
博士, 北京: 中国科学院大学, 2012
作者:  郝晓丹
收藏  |  浏览/下载:10/0  |  提交时间:2012/12/17
A study of familial MELAS: Evaluation of A3243G mutation, clinical phenotype, and magnetic resonance spectroscopy-monitored progression 期刊论文
NEUROLOGY INDIA, 2012, 卷号: 60, 期号: 1
作者:  Chen, Chunnuan;  Xiong, Nian;  Wang, Yuhui;  Xiong, Jing;  Huang, Jinsha
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/05
Human mitochondrial tRNA modification and inherited encephalomyopathies 期刊论文
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2006, 卷号: 33, 期号: 5, 页码: 418-422
作者:  Hao, R;  Wang, ED
收藏  |  浏览/下载:18/0  |  提交时间:2015/07/22


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