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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
scientific article
Author/s
author: Cristina Dallabona, Federica Invernizzi, Claudia Donnini, Daniele Ghezzi, Massimo Zeviani, Costanza Lamperti
Work details
Publication date
September 23, 2013
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Language
English
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