Author:
Barboni Piero,Carbonelli Michele,Savini Giacomo,Foscarini Beatrice,Parisi Vincenzo,Valentino Maria L.,Carta Arturo,Negri Annamaria De,Sadun Federico,Zeviani Massimo,Sadun Alfredo A.,Schimpf Simone,Wissinger Bernd,Carelli Valerio
Reference38 articles.
1. Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families;Kjer;Acta Ophthalmol Suppl,1959
2. Hereditary optic neuropathies;Newman,2005
3. Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy;Votruba;J Med Genet,1998
4. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog Ret Eye Res,2004
5. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000
Cited by
54 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献