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A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, and severe reduction of mitochondrial complex III activity

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author: Massimo Zeviani  Claudia Donnini  Costanza Lamperti  Federica Invernizzi  Daniele Ghezzi  Cristina Dallabona 

Publication date September 23, 2013
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