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LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century

✍ Scribed by Suzanne Lesage; Anne-Louise Leutenegger; Pablo Ibanez; Sabine Janin; Ebba Lohmann; Alexandra Dürr; Alexis Brice


Book ID
117854647
Publisher
American Society of Human Genetics
Year
2005
Tongue
English
Weight
765 KB
Volume
77
Category
Article
ISSN
0002-9297

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