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Acin-Perez Rebeca
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http://hub.abes.fr/oup/periodical/brainj/2010/volume_133/issue_3/101093brainawq015/authorship/4
http://hub.abes.fr/oup/periodical/brainj/2010/volume_133/issue_3/101093brainawq023/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2003/volume_12/issue_3/101093hmgddg021/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_1/101093hmgddp477/authorship/3
http://hub.abes.fr/oup/periodical/nar/2003/volume_31/issue_18/101093nargkg739/authorship/2
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Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2
Mitochondrial DNA mutations affect calcium handling in differentiated neurons
Revisiting the mouse mitochondrial DNA sequence
An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA
Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations
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