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Mayer B 1
Showing records 1 to 1 | Display all abstracts from Mayer B51700 A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Weishaupt JH; Waibel S; Birve A; Volk AE; Mayer B; Meyer T; Ludolph AC; Andersen PM
Neurobiology of Aging 2013; 34: 1516.e9-1516.e15
