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CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder

Article ID Journal Published Year Pages File Type
10215426 European Journal of Paediatric Neurology 2018 8 Pages PDF
Keywords
Lactic acidosisMultisystem diseasePhenotypeMitochondrialHereditary neuropathyGenotype
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Preview
CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder
Authors
Josef Finsterer, Ana C. Fiorini, Carla A. Scorza, Fulvio A. Scorza,
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Journal
European Journal of Paediatric Neurology
Journal: European Journal of Paediatric Neurology
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