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Your search keyword '"Calvo, Sarah"' showing total 4 results

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4 results on '"Calvo, Sarah"'

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1. Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

2. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

3. MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

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