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    A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

    A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability by Majida eCharif, Majida eCharif, Agathe eRoubertie, Sara eSalime, Sonia eMamouni, Cyril eGoizet, Christian Paul Hamel, Christian Paul Hamel, Guy eLenaers, Guy eLenaers

    Published 2015-10-01
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