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Novel alpha-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinsons disease-type pathology

Folia Med

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In particular, a study of the metabolome and of mitochondrial function in a small group of children with 22q11.2DS revealed a distinct biochemical profile, which was consistent with increased oxidative stress, and shared features with congenital propionic and/or methylmalonic acidaemia (6)

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When reconstituting, direct the stream of water along the glass wall rather than directly into the powder