LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century
- 1 August 2005
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 77 (2), 330-332
- https://doi.org/10.1086/432422
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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