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doi.org/10.1016/S0304-3940(99)00465-6, hdl.handle.net/1765/68228
Neuroscience Letters
Department of Clinical Genetics

Harhangi, B.S, Farrer, M.J, Lincoln, N, Bonifati, V, Meco, G, de Michele, G, … Breteler, M.M.B. (1999). The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease. Neuroscience Letters, 270(1), 1–4. doi:10.1016/S0304-3940(99)00465-6