Rezultati - Agnès Müller

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  1. 1
    OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

    OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model od Emmanuelle Sarzi, Marie Seveno, Camille Piro-Mégy, Lucie Elzière, Mélanie Quilès, Marie O. Péquignot, Agnès Müller, Christian Hamel, Guy Lenaers, Cécile Delettre

    Izdano 2018
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    Artigo
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  2. 2
    Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy

    Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy od Camille Piro-Mégy, Emmanuelle Sarzi, Aleix Tarrés-Solé, Marie O. Péquignot, Fenna Hensen, Mélanie Quilès, Gaël Manès, Arka Chakraborty, Audrey Sénéćhal, Béatrice Bocquet, Chantal Cazevieille, Agathe Roubertie, Agnès Müller, Majida Charif, David Goudenège, Guy Lenaers, Helmut Wilhelm, Ulrich Kellner, Nicole Weisschuh, Bernd Wissinger, Xavier Zanlonghi, Christian Hamel, Johannes N. Spelbrink, Marı́a Solà, Cécile Delettre

    Izdano 2019
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