Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
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4. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig–Hoffmann disease) and type III (Kugelberg–Welander disease);Fried;Clin Genet,1971
5. Zwei frühinfantile hereditäre Fälle von progressiver Muskelatrophie unter dem Bilde der Dystrophie, aber auf neurotischer Grundlage;Werdnig;Archic fur Psychiatrie and Nervenkrankheiten, Berlin,1891
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