Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy.
作者信息
Finsterer Josef, Zarrouk-Mahjoub Sinda
机构信息
Hospital Rudolfstiftung, Austria.
University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia.
出版信息
Intern Med. 2017 Oct 1;56(19):2693. doi: 10.2169/internalmedicine.8820-17. Epub 2017 Sep 6.
Abstract
摘要
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本文引用的文献
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Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.
Intern Med. 2017;56(1):95-99. doi: 10.2169/internalmedicine.56.7301. Epub 2017 Jan 1.
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