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Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia 
Nagel, Gabriele et al. (2013)
Wissenschaftlicher Artikel

A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany 
Weishaupt, Jochen H. et al. (2013)
Wissenschaftlicher Artikel


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FacultyMedizinische Fakultät (2)Institution
Institut für Epidemiologie und Medizinische Biometrie (2)
UKU. Klinik für Neurologie (2)
UKU. Institut für Humangenetik (1)PersonLudolph, Albert C. (2)ALS Registry Study Grp (1)Andersen, Peter M. (1)... View MoreResource type
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2013 (2)
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