An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect (Q36358437)
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English | An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect |
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An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect (English)
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Alexandre Janer
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Hana Antonicka
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Emilie Lalonde
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Tamiko Nishimura
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Florin Sasarman
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Garry K Brown
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Ruth M Brown
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Jacek Majewski
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Eric A Shoubridge
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27 September 2012
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737-743
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Identifiers
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