Multiple system atrophy (MSA) is a rare adult-onset rapidly progressive fatal neurodegenerative disorder characterized by the abnormal aggregation of misfolded α-synuclein primarily in oligodendrocytes.1 Acknowledgment: The authors thank the patients with MSA who donated their organs and Dr. Tatiana Bakaeva for her help with the autopsies.
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Mendoza‐Santiesteban et al. (2017) studied this question.
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