Investigación clínica y de laboratorio de la sospecha de trastorno del mtDNA. LCR, líquido cefalorraquídeo; ECG, electrocardiograma; EEG, electroencefalograma;

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Investigación clínica y de laboratorio de la sospecha de trastorno del mtDNA. LCR, líquido cefalorraquídeo; ECG, electrocardiograma; EEG, electroencefalograma; EMG, electromiograma; MELAS, miopatía mitocondrial, encefalopatía, acidosis láctica y episodios similares a apoplejía; MERRF, epilepsia mioclónica con fibras musculares estriadas rasgadas; LHON, neuropatía óptica hereditaria de Leber; PCR, reacción en cadena de polimerasa; RFLP, polimorfismo de la longitud de fragmentos de restricción (restriction fragment length polymorphism). De: DNA mitocondrial y enfermedades y rasgos hereditarios, Harrison. Principios de Medicina Interna, 18e Citación: Longo DL, Kasper DL, Jameson J, Fauci AS, Hauser SL, Loscalzo J. Harrison. Principios de Medicina Interna, 18e; 2012 En: http://accessmedicina.mhmedical.com/DownloadImage.aspx?image=/data/books/1622/harrison_e_ch18_fig-18-06.png&sec=101837678&BookID=1622&ChapterSecID=101837634&imagename= Recuperado: October 24, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved

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