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B.S. Harhangi (Biswadjiet), M.J. Farrer (Matthew), N. Lincoln (Nadina), V. Bonifati (Vincenzo), G. Meco (Giuseppe), G. de Michele (Giuseppe), A. Brice, A. Durr, M. Martinez (Maria), T. Gasser (Thomas), et al. B. Bereznai (Benjamin), J. Vaughan (Jenny), N.W. Wood (Nicholas), J. Hardy (John), B.A. Oostra (Ben) and M.M.B. Breteler (Monique)

1999-07-23

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

Publication

Publication

Neuroscience Letters , Volume 270 - Issue 1 p. 1- 4

Additional Metadata
Keywords Candidate gene, Family studies, Genetics, Parkinson's disease, Ubiquitin-carboxy-terminal-hydrolase- L1
Persistent URL doi.org/10.1016/S0304-3940(99)00465-6, hdl.handle.net/1765/68228
Journal Neuroscience Letters
Organisation Department of Clinical Genetics


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