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  1. 1
    Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclear MTO1 and a mitochondrial MT-TF variant

    Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclear MTO1 and a mitochondrial MT-TF variant von Charif, Majida, Titah, Salah Mohamed Cherif, Roubertie, Agathe, Desquiret-Dumas, Valérie, Gueguen, Naig, Meunier, Isabelle, Leid, Jean, Massal, Frédéric, Zanlonghi, Xavier, Mercier, Jacques, Raynaud de Mauverger, Eric, Procaccio, Vincent, de Camaret, Bénédicte Mousson, Lenaers, Guy, Hamel, Christian P.


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  2. 2
    Cataract as a Phenotypic Marker for a Mutation in WFS1, the Wolfram Syndrome Gene

    Cataract as a Phenotypic Marker for a Mutation in WFS1, the Wolfram Syndrome Gene von Cherif Titah, Salah Mohamed, Meunier, Isabelle, Blanchet, Catherine, Lopez, Severine, Rondouin, Gerard, Lenaers, Guy, Amati-Bonneau, Patrizia, Reynier, Pascal, Paquis-Flucklinger, Veronique, Hamel, Christian P.


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