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

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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
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Harhangi, B., Farrer, M., Lincoln, N., Bonifati, V., Meco, G., de Michele, G., Brice, A., Durr, A., Martinez, M., Gasser, T., Bereznai, B., Vaughan, J., Wood, N., Hardy, J., Oostra, B.& Breteler, M. (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.https://doi.org/10.1016/S0304-3940(99)00465-6

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