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Dive into the research topics of 'Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.'. Together they form a unique fingerprint.- Sort by
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Olivier Baris, Cécile Delettre, Patrizia Amati-Bonneau, Marie Odile Surget, Jean François Charlin, Antoine Catier, Laurence Derieux, Jean Laurent Guyomard, Hélène Dollfus, Philippe Jonveaux, Carmen Ayuso, Irene Maumenee, Birgit Lorenz, Shehla Mohammed, Yves Tourmen, Dominique Bonneau, Yves Malthièry, Christian Hamel, Pascal Reynier
Research output: Contribution to journal › Article › peer-review