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Research | 6 February 2018 | Open
OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model
- Emmanuelle Sarzi
- , Marie Seveno
- , Camille Piro-Mégy
- , Lucie Elzière
- , Mélanie Quilès
- , Marie Péquignot
- , Agnès Müller
- , Christian P. Hamel
- , Guy Lenaers
- & Cécile Delettre
Scientific Reports 8 , 1–6

Rights & permissionsfor article OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model . Opens in a new window.
Research | 7 May 2007
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion
Nature Genetics 39 , 776–780

Rights & permissionsfor article Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion . Opens in a new window.
Research | 2 April 2006
MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion
- Antonella Spinazzola
- , Carlo Viscomi
- , Erika Fernandez-Vizarra
- , Franco Carrara
- , Pio D'Adamo
- , Sarah Calvo
- , René Massimiliano Marsano
- , Claudia Donnini
- , Hans Weiher
- , Pietro Strisciuglio
- , Rossella Parini
- , Emmanuelle Sarzi
- , Alicia Chan
- , Salvatore DiMauro
- , Agnes Rötig
- , Paolo Gasparini
- , Iliana Ferrero
- , Vamsi K Mootha
- , Valeria Tiranti
- & Massimo Zeviani
Nature Genetics 38 , 570–575

Rights & permissionsfor article MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion . Opens in a new window.

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OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

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

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