Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus

<div>Methylamine tungstate, negatively stained, whole-mount TEM analysis of mitochondria (mt) isolated from the patient’s plasma. Mitochondria with different shapes and sizes, ranging from ∼400 nm (Panel (a)) to over 1 <i>µ</i>m (Panel (f)), were identified. Some mitochondria are attached to “vesicle-like” structures protruding from the membrane (∼100 nm in diameter), pointed by white arrows in Panels (a–c). Scale bar: 100 nm.</div>

Case Reports in Genetics

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Figure 3

Figure 3: Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus 

Figure 3 | Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus 