Citations
1 citation(s) found for "Willvonseder, R".
A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism
Willvonseder, R, Goldstein, Norman, Yoss, Robert E., Tauxe, W. Newlon, McCall, John
Neurology | May 13, 2012 | Volume: 23 | Issue: 10 | Pages: 1039-1039
