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Severe atrophy of the cerebellum on magnetic resonance imaging in a Chinese patient with maternally inherited diabetes and deafness with the A3243G mitochondrial DNA mutation

Crossref DOI link: https://doi.org/10.1007/s13410-015-0384-2

Published Online: 2015-04-15

Published Print: 2015-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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