Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Mitochondrial Encephalomyopathies and MELAS[original query] |
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[The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies]. Zhonghua yi xue za zhi 2002 1 81 (11): 659-61. Song D, Zhang Y, Shi |
Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies. Chinese medical journal 2002 1 114 (12): 1273-5. Song D, Zhang Y, Shi J, Lü Q, Chen J, Zhang H, Zhang W, Wang H, Cai |
[Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2005 Feb 27 (1): 77-80. Zhang Ying, Wang Zhao-xia, Niu Shu-lan, Xu Yu-feng, Pei Pei, Yuan Yun, Yang Yan-ling, Qi |
[Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies]. Zhonghua yi xue za zhi 2011 Apr 91 (14): 969-72. Xu Jian-biao, Ma Yi-nan, Pan Hong, Zheng Xue-fei, Zhang Ying, Wang Song-tao, Bu Ding-fang, Qi |
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- Page last updated:May 06, 2024
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